Linked Data
ClinVar Variation Id:
367514
dbSNP Id:
rs56302651
ExAC:
9:94495624 G / A
gnomAD v2:
9-94495624-G-A
gnomAD v3:
9-91733342-G-A
gnomAD v4:
9-91733342-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.91733342G>A , CM000671.2:g.91733342G>A | GRCh38 |
| NC_000009.11:g.94495624G>A , CM000671.1:g.94495624G>A | GRCh37 |
| NC_000009.10:g.93535445G>A | NCBI36 |
| NG_008089.1:g.221821C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375708.4:c.717C>T MANE Select | ENSP00000364860.3:p.Cys239= | |
| ENST00000375708.3:c.717C>T | ENSP00000364860.3:p.Cys239= | |
| ENST00000375715.5:c.297C>T | ENSP00000364867.1:p.Cys99= | |
| ENST00000550066.5:n.1185C>T | ||
| NM_004560.3:c.717C>T | NP_004551.2:p.Cys239= | |
| XM_005252008.3:c.297C>T | XP_005252065.1:p.Cys99= | |
| XM_006717121.2:c.297C>T | XP_006717184.1:p.Cys99= | |
| XM_011518721.1:c.297C>T | XP_011517023.1:p.Cys99= | |
| NM_001318204.1:c.717C>T | NP_001305133.1:p.Cys239= | |
| XM_005252008.4:c.297C>T | XP_005252065.1:p.Cys99= | |
| XM_006717121.3:c.297C>T | XP_006717184.1:p.Cys99= | |
| XM_017014762.1:c.708C>T | XP_016870251.1:p.Cys236= | |
| XM_017014763.1:c.297C>T | XP_016870252.1:p.Cys99= | |
| XR_001746315.1:n.960C>T | ||
| NM_004560.4:c.717C>T MANE Select | NP_004551.2:p.Cys239= | |
| NM_001318204.2:c.717C>T | NP_001305133.1:p.Cys239= |