Linked Data
dbSNP Id:
rs996055967
gnomAD v2:
17-73515019-C-T
gnomAD v3:
17-75518938-C-T
gnomAD v4:
17-75518938-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.75518938C>T , CM000679.2:g.75518938C>T | GRCh38 |
| NC_000017.10:g.73515019C>T , CM000679.1:g.73515019C>T | GRCh37 |
| NC_000017.9:g.71026614C>T | NCBI36 |
| NG_013041.1:g.7411C>T | |
| NG_033152.1:g.1646G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333213.11:c.469-57C>T MANE Select | ENSP00000327487.6:n.469-57C>T | |
| ENST00000434205.8:c.166-57C>T | ENSP00000406559.4:n.166-57C>T | |
| ENST00000545228.3:c.469-57C>T | ENSP00000438169.3:n.469-57C>T | |
| ENST00000579449.2:n.268-57C>T | ||
| ENST00000580013.6:n.478-57C>T | ||
| ENST00000583818.2:c.469-57C>T | ENSP00000461928.2:n.469-57C>T | |
| ENST00000679370.1:n.856-57C>T | ||
| ENST00000679429.1:c.469-65C>T | ENSP00000505403.1:n.469-65C>T | |
| ENST00000679443.1:n.344-57C>T | ||
| ENST00000679782.1:c.469-57C>T | ENSP00000505995.1:n.469-57C>T | |
| ENST00000679919.1:n.344-57C>T | ||
| ENST00000679928.1:c.469-57C>T | ENSP00000506071.1:n.469-57C>T | |
| ENST00000680528.1:n.494-57C>T | ||
| ENST00000680999.1:c.469-57C>T | ENSP00000504984.1:n.469-57C>T | |
| ENST00000681282.1:c.469-57C>T | ENSP00000506339.1:n.469-57C>T | |
| ENST00000333213.10:c.469-57C>T | ENSP00000327487.6:n.469-57C>T | |
| ENST00000434205.7:c.166-57C>T | ENSP00000406559.3:n.166-57C>T | |
| ENST00000578415.1:c.429-57C>T | ||
| ENST00000580013.5:n.494-65C>T | ||
| ENST00000583173.5:c.304-57C>T | ENSP00000463619.1:n.304-57C>T | |
| ENST00000583818.1:c.364-57C>T | ENSP00000461928.1:n.364-57C>T | |
| NM_207346.2:c.469-57C>T | NP_997229.2:n.469-57C>T | |
| XM_005257229.2:c.469-57C>T | XP_005257286.1:n.469-57C>T | |
| XM_006721821.2:c.166-57C>T | XP_006721884.1:n.166-57C>T | |
| XM_011524616.1:c.469-57C>T | XP_011522918.1:n.469-57C>T | |
| XM_011524617.1:c.469-57C>T | XP_011522919.1:n.469-57C>T | |
| XM_011524618.1:c.469-57C>T | XP_011522920.1:n.469-57C>T | |
| XR_243646.2:n.499-57C>T | ||
| XM_005257229.4:c.469-57C>T | XP_005257286.1:n.469-57C>T | |
| XR_243646.4:n.505-57C>T | ||
| NM_207346.3:c.469-57C>T MANE Select | NP_997229.2:n.469-57C>T |