Linked Data
MyVariant Identifiers:
chr9:g.137300072C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.134408226C>T , CM000671.2:g.134408226C>T | GRCh38 |
| NC_000009.11:g.137300072C>T , CM000671.1:g.137300072C>T | GRCh37 |
| NC_000009.10:g.136439893C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000481739.2:c.357C>T MANE Select | ENSP00000419692.1:p.Val119= | |
| ENST00000672570.1:c.276C>T | ENSP00000500402.1:p.Val92= | |
| ENST00000356384.4:n.767C>T | ||
| ENST00000481739.1:c.357C>T | ENSP00000419692.1:p.Val119= | |
| NM_001291920.1:c.276C>T | NP_001278849.1:p.Val92= | |
| NM_001291921.1:c.66C>T | NP_001278850.1:p.Val22= | |
| NM_002957.5:c.357C>T | NP_002948.1:p.Val119= | |
| NM_002957.6:c.357C>T MANE Select | NP_002948.1:p.Val119= | |
| NM_001291921.2:c.66C>T | NP_001278850.1:p.Val22= | |
| NM_001291920.2:c.276C>T | NP_001278849.1:p.Val92= |