HGVS | Genome Assembly |
---|---|
NC_000006.12:g.151618522T>G , CM000668.2:g.151618522T>G | GRCh38 |
NC_000006.11:g.151939657T>G , CM000668.1:g.151939657T>G | GRCh37 |
NC_000006.10:g.151981350T>G | NCBI36 |
NG_021198.1:g.129483T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000239374.8:c.*375T>G MANE Select | ENSP00000239374.6:n.*375T>G | |
ENST00000239374.7:c.*375T>G | ENSP00000239374.6:n.*375T>G | |
NM_025059.3:c.*375T>G | NP_079335.2:n.*375T>G | |
XM_011536147.1:c.*375T>G | XP_011534449.1:n.*375T>G | |
XM_011536148.1:c.*375T>G | XP_011534450.1:n.*375T>G | |
XM_011536147.2:c.*375T>G | XP_011534449.1:n.*375T>G | |
XM_011536148.2:c.*375T>G | XP_011534450.1:n.*375T>G | |
NM_025059.4:c.*375T>G MANE Select | NP_079335.2:n.*375T>G |