HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204190368C>T , CM000663.2:g.204190368C>T | GRCh38 |
NC_000001.10:g.204159496C>T , CM000663.1:g.204159496C>T | GRCh37 |
NC_000001.9:g.202426119C>T | NCBI36 |
NG_032151.1:g.11124G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367194.5:c.*116G>A MANE Select | ENSP00000356162.4:n.*116G>A | |
ENST00000367194.4:c.*116G>A | ENSP00000356162.4:n.*116G>A | |
NM_002256.3:c.*116G>A | NP_002247.3:n.*116G>A | |
XM_011509525.1:c.*116G>A | XP_011507827.1:n.*116G>A | |
NM_002256.4:c.*116G>A MANE Select | NP_002247.3:n.*116G>A |