Linked Data
dbSNP Id:
rs1404660638
gnomAD v2:
19-41928874-C-A
gnomAD v3:
19-41422969-C-A
gnomAD v4:
19-41422969-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.41422969C>A , CM000681.2:g.41422969C>A | GRCh38 |
| NC_000019.9:g.41928874C>A , CM000681.1:g.41928874C>A | GRCh37 |
| NC_000019.8:g.46620714C>A | NCBI36 |
| NG_013004.1:g.30181C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000269980.7:c.996-29C>A MANE Select | ENSP00000269980.2:n.996-29C>A | |
| ENST00000269980.6:c.996-29C>A | ENSP00000269980.2:n.996-29C>A | |
| ENST00000457836.6:c.976C>A | ENSP00000416000.2:p.Leu326Met | |
| ENST00000540732.3:c.1098-29C>A | ENSP00000443246.1:n.1098-29C>A | |
| ENST00000542943.5:c.909-29C>A | ENSP00000440345.1:n.909-29C>A | |
| ENST00000595085.5:c.922+272C>A | ENSP00000471150.2:n.922+272C>A | |
| NM_000709.3:c.996-29C>A | NP_000700.1:n.996-29C>A | |
| NM_001164783.1:c.993-29C>A | NP_001158255.1:n.993-29C>A | |
| NM_000709.4:c.996-29C>A MANE Select | NP_000700.1:n.996-29C>A | |
| NM_001164783.2:c.993-29C>A | NP_001158255.1:n.993-29C>A |