Linked Data
dbSNP Id:
rs974693257
gnomAD v2:
19-41930236-G-A
gnomAD v3:
19-41424331-G-A
gnomAD v4:
19-41424331-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.41424331G>A , CM000681.2:g.41424331G>A | GRCh38 |
| NC_000019.9:g.41930236G>A , CM000681.1:g.41930236G>A | GRCh37 |
| NC_000019.8:g.46622076G>A | NCBI36 |
| NG_013004.1:g.31543G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000269980.7:c.1168-107G>A MANE Select | ENSP00000269980.2:n.1168-107G>A | |
| ENST00000269980.6:c.1168-107G>A | ENSP00000269980.2:n.1168-107G>A | |
| ENST00000457836.6:c.1177-107G>A | ENSP00000416000.2:n.1177-107G>A | |
| ENST00000540732.3:c.1270-107G>A | ENSP00000443246.1:n.1270-107G>A | |
| ENST00000544905.1:c.62-171G>A | ||
| ENST00000595085.5:c.922+1634G>A | ENSP00000471150.2:n.922+1634G>A | |
| NM_000709.3:c.1168-107G>A | NP_000700.1:n.1168-107G>A | |
| NM_001164783.1:c.1165-107G>A | NP_001158255.1:n.1165-107G>A | |
| NM_000709.4:c.1168-107G>A MANE Select | NP_000700.1:n.1168-107G>A | |
| NM_001164783.2:c.1165-107G>A | NP_001158255.1:n.1165-107G>A |