Linked Data
ClinVar Variation Id:
376610
ClinVar RCV Id:
RCV000420116
RCV000419821
RCV000421694
RCV000423899
RCV000426383
RCV000424030
RCV000425288
RCV000430612
RCV000430072
RCV000431709
RCV000431956
RCV000436443
RCV000437679
RCV000436622
RCV000440707
RCV000441771
RCV000443866
RCV000444860
RCV000444992
RCV001851020
RCV002348144
RCV003470376
RCV002465649
RCV003335320
dbSNP Id:
rs587780070
PubMed:
PMID:26619011
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7675077G>C , CM000679.2:g.7675077G>C | GRCh38 |
| NC_000017.10:g.7578395G>C , CM000679.1:g.7578395G>C | GRCh37 |
| NC_000017.9:g.7519120G>C | NCBI36 |
| NG_017013.2:g.17474C>G , LRG_321:g.17474C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000503591.2:c.535C>G | ENSP00000426252.2:p.His179Asp | |
| ENST00000508793.6:c.535C>G | ENSP00000424104.2:p.His179Asp | |
| ENST00000509690.6:c.139C>G | ENSP00000425104.2:p.His47Asp | |
| ENST00000514944.6:c.256C>G | ENSP00000423862.2:p.His86Asp | |
| ENST00000604348.6:c.514C>G | ENSP00000473895.2:p.His172Asp | |
| ENST00000269305.9:c.535C>G MANE Select | ENSP00000269305.4:p.His179Asp | |
| ENST00000269305.8:c.535C>G | ENSP00000269305.4:p.His179Asp | |
| ENST00000359597.8:c.535C>G | ENSP00000352610.4:p.His179Asp | |
| ENST00000413465.6:c.535C>G | ENSP00000410739.2:p.His179Asp | |
| ENST00000420246.6:c.535C>G | ENSP00000391127.2:p.His179Asp | |
| ENST00000445888.6:c.535C>G | ENSP00000391478.2:p.His179Asp | |
| ENST00000455263.6:c.535C>G | ENSP00000398846.2:p.His179Asp | |
| ENST00000504290.5:c.139C>G | ENSP00000484409.1:p.His47Asp | |
| ENST00000504937.5:c.139C>G | ENSP00000481179.1:p.His47Asp | |
| ENST00000505014.5:n.791C>G | ||
| ENST00000509690.5:c.139C>G | ENSP00000425104.1:p.His47Asp | |
| ENST00000510385.5:c.139C>G | ENSP00000478499.1:p.His47Asp | |
| ENST00000514944.5:c.256C>G | ENSP00000423862.1:p.His86Asp | |
| ENST00000574684.1:n.43C>G | ||
| ENST00000610292.4:c.418C>G | ENSP00000478219.1:p.His140Asp | |
| ENST00000610538.4:c.418C>G | ENSP00000480868.1:p.His140Asp | |
| ENST00000610623.4:c.58C>G | ENSP00000477531.1:p.His20Asp | |
| ENST00000615910.4:c.502C>G | ENSP00000482903.1:p.His168Asp | |
| ENST00000617185.4:c.535C>G | ENSP00000482258.1:p.His179Asp | |
| ENST00000618944.4:c.58C>G | ENSP00000481401.1:p.His20Asp | |
| ENST00000619186.4:c.58C>G | ENSP00000484375.1:p.His20Asp | |
| ENST00000619485.4:c.418C>G | ENSP00000482537.1:p.His140Asp | |
| ENST00000620739.4:c.418C>G | ENSP00000481638.1:p.His140Asp | |
| ENST00000622645.4:c.418C>G | ENSP00000482222.1:p.His140Asp | |
| ENST00000635293.1:c.418C>G | ENSP00000488924.1:p.His140Asp | |
| NM_000546.5:c.535C>G , LRG_321t1:c.535C>G | NP_000537.3:p.His179Asp | |
| NM_001126112.2:c.535C>G , LRG_321t2:c.535C>G | NP_001119584.1:p.His179Asp | |
| NM_001126113.2:c.535C>G , LRG_321t4:c.535C>G | NP_001119585.1:p.His179Asp | |
| NM_001126114.2:c.535C>G , LRG_321t3:c.535C>G | NP_001119586.1:p.His179Asp | |
| NM_001126115.1:c.139C>G , LRG_321t5:c.139C>G | NP_001119587.1:p.His47Asp | |
| NM_001126116.1:c.139C>G , LRG_321t6:c.139C>G | NP_001119588.1:p.His47Asp | |
| NM_001126117.1:c.139C>G , LRG_321t7:c.139C>G | NP_001119589.1:p.His47Asp | |
| NM_001126118.1:c.418C>G , LRG_321t8:c.418C>G | NP_001119590.1:p.His140Asp | |
| NM_001276695.1:c.418C>G | NP_001263624.1:p.His140Asp | |
| NM_001276696.1:c.418C>G | NP_001263625.1:p.His140Asp | |
| NM_001276697.1:c.58C>G | NP_001263626.1:p.His20Asp | |
| NM_001276698.1:c.58C>G | NP_001263627.1:p.His20Asp | |
| NM_001276699.1:c.58C>G | NP_001263628.1:p.His20Asp | |
| NM_001276760.1:c.418C>G | NP_001263689.1:p.His140Asp | |
| NM_001276761.1:c.418C>G | NP_001263690.1:p.His140Asp | |
| NM_001276695.2:c.418C>G | NP_001263624.1:p.His140Asp | |
| NM_001276696.2:c.418C>G | NP_001263625.1:p.His140Asp | |
| NM_001276697.2:c.58C>G | NP_001263626.1:p.His20Asp | |
| NM_001276698.2:c.58C>G | NP_001263627.1:p.His20Asp | |
| NM_001276699.2:c.58C>G | NP_001263628.1:p.His20Asp | |
| NM_001276760.2:c.418C>G | NP_001263689.1:p.His140Asp | |
| NM_001276761.2:c.418C>G | NP_001263690.1:p.His140Asp | |
| NM_000546.6:c.535C>G MANE Select | NP_000537.3:p.His179Asp | |
| NM_001126112.3:c.535C>G | NP_001119584.1:p.His179Asp | |
| NM_001126113.3:c.535C>G | NP_001119585.1:p.His179Asp | |
| NM_001126114.3:c.535C>G | NP_001119586.1:p.His179Asp | |
| NM_001126115.2:c.139C>G | NP_001119587.1:p.His47Asp | |
| NM_001126116.2:c.139C>G | NP_001119588.1:p.His47Asp | |
| NM_001126117.2:c.139C>G | NP_001119589.1:p.His47Asp | |
| NM_001126118.2:c.418C>G | NP_001119590.1:p.His140Asp | |
| NM_001276695.3:c.418C>G | NP_001263624.1:p.His140Asp | |
| NM_001276696.3:c.418C>G | NP_001263625.1:p.His140Asp | |
| NM_001276697.3:c.58C>G | NP_001263626.1:p.His20Asp | |
| NM_001276698.3:c.58C>G | NP_001263627.1:p.His20Asp | |
| NM_001276699.3:c.58C>G | NP_001263628.1:p.His20Asp | |
| NM_001276760.3:c.418C>G | NP_001263689.1:p.His140Asp | |
| NM_001276761.3:c.418C>G | NP_001263690.1:p.His140Asp |