Linked Data
ClinVar Variation Id:
1088098
ClinVar RCV Id:
RCV001406439
dbSNP Id:
rs947267758
gnomAD v2:
1-15772229-C-T
gnomAD v4:
1-15445734-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.15445734C>T , CM000663.2:g.15445734C>T | GRCh38 |
| NC_000001.10:g.15772229C>T , CM000663.1:g.15772229C>T | GRCh37 |
| NC_000001.9:g.15644816C>T | NCBI36 |
| NG_009253.1:g.12292C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375949.5:c.777C>T MANE Select | ENSP00000365116.4:p.Ile259= | |
| ENST00000375943.6:c.*231C>T | ENSP00000365110.2:n.*231C>T | |
| ENST00000375949.4:c.777C>T | ENSP00000365116.4:p.Ile259= | |
| ENST00000483406.1:n.541C>T | ||
| NM_007272.2:c.777C>T | NP_009203.2:p.Ile259= | |
| XM_011540550.1:c.631C>T | XP_011538852.1:p.Arg211Ter | |
| NM_007272.3:c.777C>T MANE Select | NP_009203.2:p.Ile259= |