Linked Data
ClinVar Variation Id:
41549
ClinVar RCV Id:
RCV000034440
RCV000044377
RCV000120339
RCV000083103
RCV000162541
RCV000735549
RCV001353826
dbSNP Id:
rs28897727
ExAC:
13:32912750 G / T
gnomAD v2:
13-32912750-G-T
gnomAD v3:
13-32338613-G-T
gnomAD v4:
13-32338613-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.32338613G>T , CM000675.2:g.32338613G>T | GRCh38 |
| NC_000013.10:g.32912750G>T , CM000675.1:g.32912750G>T | GRCh37 |
| NC_000013.9:g.31810750G>T | NCBI36 |
| NG_012772.3:g.28134G>T , LRG_293:g.28134G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000470094.2:c.4258G>T | ENSP00000434898.2:p.Asp1420Tyr | |
| ENST00000528762.2:c.4258G>T | ENSP00000433168.2:p.Asp1420Tyr | |
| ENST00000530893.7:c.3889G>T | ENSP00000499438.2:p.Asp1297Tyr | |
| ENST00000665585.2:c.4258G>T | ENSP00000499570.2:p.Asp1420Tyr | |
| ENST00000666593.2:c.4258G>T | ENSP00000499256.2:p.Asp1420Tyr | |
| ENST00000700202.2:c.4258G>T | ENSP00000514856.2:p.Asp1420Tyr | |
| ENST00000380152.8:c.4258G>T MANE Select | ENSP00000369497.3:p.Asp1420Tyr | |
| ENST00000544455.6:c.4258G>T | ENSP00000439902.1:p.Asp1420Tyr | |
| ENST00000614259.2:c.4258G>T | ENSP00000506251.1:p.Asp1420Tyr | |
| ENST00000680887.1:c.4258G>T | ENSP00000505508.1:p.Asp1420Tyr | |
| ENST00000380152.7:c.4258G>T | ENSP00000369497.3:p.Asp1420Tyr | |
| ENST00000544455.5:c.4258G>T | ENSP00000439902.1:p.Asp1420Tyr | |
| ENST00000614259.1:n.4258G>T | ||
| NM_000059.3:c.4258G>T , LRG_293t1:c.4258G>T | NP_000050.2:p.Asp1420Tyr | |
| XM_011535203.1:c.4258G>T | XP_011533505.1:p.Asp1420Tyr | |
| XM_011535204.1:c.4258G>T | XP_011533506.1:p.Asp1420Tyr | |
| XM_011535205.1:c.4258G>T | XP_011533507.1:p.Asp1420Tyr | |
| NM_000059.4:c.4258G>T MANE Select | NP_000050.3:p.Asp1420Tyr |