Linked Data
dbSNP Id:
rs772324528
ExAC:
19:47207714 C / A
gnomAD v2:
19-47207714-C-A
gnomAD v3:
19-46704457-C-A
gnomAD v4:
19-46704457-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.46704457C>A , CM000681.2:g.46704457C>A | GRCh38 |
| NC_000019.9:g.47207714C>A , CM000681.1:g.47207714C>A | GRCh37 |
| NC_000019.8:g.51899554C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291281.9:c.666+38G>T MANE Select | ENSP00000291281.3:n.666+38G>T | |
| ENST00000291281.8:c.666+38G>T | ENSP00000291281.3:n.666+38G>T | |
| ENST00000433867.5:c.666+38G>T | ENSP00000393978.1:n.666+38G>T | |
| ENST00000595515.5:c.666+38G>T | ENSP00000470804.1:n.666+38G>T | |
| ENST00000597641.1:c.401+38G>T | ENSP00000469064.1:n.401+38G>T | |
| ENST00000600194.5:c.195+38G>T | ENSP00000472744.1:n.195+38G>T | |
| ENST00000601605.5:c.41-3345G>T | ENSP00000470442.1:n.41-3345G>T | |
| ENST00000601806.5:c.195+38G>T | ENSP00000469106.1:n.195+38G>T | |
| NM_001079880.1:c.666+38G>T | NP_001073349.1:n.666+38G>T | |
| NM_001079881.1:c.666+38G>T | NP_001073350.1:n.666+38G>T | |
| NM_001079882.1:c.195+38G>T | NP_001073351.1:n.195+38G>T | |
| NM_016457.4:c.666+38G>T | NP_057541.2:n.666+38G>T | |
| XM_005258716.2:c.195+38G>T | XP_005258773.2:n.195+38G>T | |
| NM_001079880.2:c.666+38G>T | NP_001073349.1:n.666+38G>T | |
| NM_001079881.2:c.666+38G>T | NP_001073350.1:n.666+38G>T | |
| NM_001079882.2:c.195+38G>T | NP_001073351.1:n.195+38G>T | |
| NM_016457.5:c.666+38G>T MANE Select | NP_057541.2:n.666+38G>T |