HGVS | Genome Assembly |
---|---|
NC_000001.11:g.229431766C>G , CM000663.2:g.229431766C>G | GRCh38 |
NC_000001.10:g.229567513C>G , CM000663.1:g.229567513C>G | GRCh37 |
NC_000001.9:g.227634136C>G | NCBI36 |
NG_006672.1:g.7331G>C , LRG_429:g.7331G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000366683.4:c.945G>C | ENSP00000355644.4:p.Met315Ile | |
ENST00000684723.1:c.810G>C | ENSP00000508084.1:p.Met270Ile | |
ENST00000366683.3:c.576G>C | ENSP00000355644.3:p.Met192Ile | |
ENST00000366684.7:c.945G>C MANE Select | ENSP00000355645.3:p.Met315Ile | |
NM_001100.3:c.945G>C , LRG_429t1:c.945G>C | NP_001091.1:p.Met315Ile | |
NM_001100.4:c.945G>C MANE Select | NP_001091.1:p.Met315Ile |