HGVS | Genome Assembly |
---|---|
NC_000010.11:g.47325319G>A , CM000672.2:g.47325319G>A | GRCh38 |
NC_000010.10:g.48414043C>T , CM000672.1:g.48414043C>T | GRCh37 |
NC_000010.9:g.48034049C>T | NCBI36 |
NG_033916.1:g.7830G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000581492.3:c.825G>A MANE Select | ENSP00000463051.1:p.Met275Ile | |
ENST00000581492.2:c.825G>A | ENSP00000463051.1:p.Met275Ile | |
NM_016204.2:c.825G>A | NP_057288.1:p.Met275Ile | |
XM_006717761.2:c.825G>A | XP_006717824.1:p.Met275Ile | |
NM_016204.3:c.825G>A | NP_057288.1:p.Met275Ile | |
NM_016204.4:c.825G>A MANE Select | NP_057288.1:p.Met275Ile |