Linked Data
MyVariant Identifiers:
chr9:g.137300090A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.134408244A>C , CM000671.2:g.134408244A>C | GRCh38 |
| NC_000009.11:g.137300090A>C , CM000671.1:g.137300090A>C | GRCh37 |
| NC_000009.10:g.136439911A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000481739.2:c.375A>C MANE Select | ENSP00000419692.1:p.Gly125= | |
| ENST00000672570.1:c.294A>C | ENSP00000500402.1:p.Gly98= | |
| ENST00000356384.4:n.785A>C | ||
| ENST00000481739.1:c.375A>C | ENSP00000419692.1:p.Gly125= | |
| NM_001291920.1:c.294A>C | NP_001278849.1:p.Gly98= | |
| NM_001291921.1:c.84A>C | NP_001278850.1:p.Gly28= | |
| NM_002957.5:c.375A>C | NP_002948.1:p.Gly125= | |
| NM_002957.6:c.375A>C MANE Select | NP_002948.1:p.Gly125= | |
| NM_001291921.2:c.84A>C | NP_001278850.1:p.Gly28= | |
| NM_001291920.2:c.294A>C | NP_001278849.1:p.Gly98= |