Linked Data
ClinVar Variation Id:
758088
ClinVar RCV Id:
RCV000935774
dbSNP Id:
rs200862223
ExAC:
9:127262948 C / T
gnomAD v2:
9-127262948-C-T
gnomAD v3:
9-124500669-C-T
gnomAD v4:
9-124500669-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.124500669C>T , CM000671.2:g.124500669C>T | GRCh38 |
| NC_000009.11:g.127262948C>T , CM000671.1:g.127262948C>T | GRCh37 |
| NC_000009.10:g.126302769C>T | NCBI36 |
| NG_008176.1:g.11752G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373588.9:c.291G>A MANE Select | ENSP00000362690.4:p.Pro97= | |
| ENST00000373587.3:c.39+279G>A | ENSP00000362689.3:n.39+279G>A | |
| ENST00000373588.8:c.291G>A | ENSP00000362690.4:p.Pro97= | |
| ENST00000455734.1:c.291G>A | ENSP00000393245.1:p.Pro97= | |
| ENST00000620110.4:c.291G>A | ENSP00000483309.1:p.Pro97= | |
| NM_004959.4:c.291G>A | NP_004950.2:p.Pro97= | |
| XM_005251871.2:c.291G>A | XP_005251928.1:p.Pro97= | |
| XM_005251872.3:c.30G>A | XP_005251929.1:p.Pro10= | |
| XM_011518455.1:c.291G>A | XP_011516757.1:p.Pro97= | |
| XM_011518456.1:c.291G>A | XP_011516758.1:p.Pro97= | |
| NM_004959.5:c.291G>A MANE Select | NP_004950.2:p.Pro97= |