Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133356453T>C , CM000671.2:g.133356453T>C | GRCh38 |
| NC_000009.10:g.135213150T>C | NCBI36 |
| NG_008477.1:g.5033A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003172.4:c.1A>G MANE Select | NP_003163.1:p.Met1Val |
| ENST00000371974.8:c.1A>G MANE Select | ENSP00000361042.3:p.Met1Val |
| NM_001280787.1:c.-275A>G | NP_001267716.1:n.-275A>G |
| NM_003172.3:c.1A>G | NP_003163.1:p.Met1Val |
| ENST00000371974.7:c.1A>G | ENSP00000361042.3:p.Met1Val |
| ENST00000463965.1:n.224A>G | |
| ENST00000615505.4:c.-275A>G | ENSP00000482067.1:n.-275A>G |