Linked Data
ClinVar Variation Id:
17849
ClinVar RCV Id:
RCV000019429
dbSNP Id:
rs121918392
ExAC:
19:45411034 G / A
gnomAD v2:
19-45411034-G-A
gnomAD v3:
19-44907777-G-A
gnomAD v4:
19-44907777-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.44907777G>A , CM000681.2:g.44907777G>A | GRCh38 |
| NC_000019.9:g.45411034G>A , CM000681.1:g.45411034G>A | GRCh37 |
| NC_000019.8:g.50102874G>A | NCBI36 |
| NG_007084.2:g.6996G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000252486.9:c.61G>A MANE Select | ENSP00000252486.3:p.Glu21Lys | |
| ENST00000252486.8:c.61G>A | ENSP00000252486.3:p.Glu21Lys | |
| ENST00000425718.1:c.61G>A | ENSP00000410423.1:p.Glu21Lys | |
| ENST00000434152.5:c.139G>A | ENSP00000413653.2:p.Glu47Lys | |
| ENST00000446996.5:c.61G>A | ENSP00000413135.1:p.Glu21Lys | |
| NM_000041.3:c.61G>A | NP_000032.1:p.Glu21Lys | |
| NM_001302688.1:c.139G>A | NP_001289617.1:p.Glu47Lys | |
| NM_001302689.1:c.61G>A | NP_001289618.1:p.Glu21Lys | |
| NM_001302690.1:c.61G>A | NP_001289619.1:p.Glu21Lys | |
| NM_001302691.1:c.61G>A | NP_001289620.1:p.Glu21Lys | |
| NM_000041.4:c.61G>A MANE Select | NP_000032.1:p.Glu21Lys | |
| NM_001302688.2:c.139G>A | NP_001289617.1:p.Glu47Lys | |
| NM_001302689.2:c.61G>A | NP_001289618.1:p.Glu21Lys | |
| NM_001302691.2:c.61G>A | NP_001289620.1:p.Glu21Lys | |
| NM_001302690.2:c.61G>A | NP_001289619.1:p.Glu21Lys |