HGVS | Genome Assembly |
---|---|
NC_000002.12:g.26135172G>T , CM000664.2:g.26135172G>T | GRCh38 |
NC_000002.11:g.26358041G>T , CM000664.1:g.26358041G>T | GRCh37 |
NC_000002.10:g.26211545G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264710.5:c.*151G>T MANE Select | ENSP00000264710.4:n.*151G>T | |
ENST00000264710.4:c.*151G>T | ENSP00000264710.4:n.*151G>T | |
ENST00000495146.5:n.1117G>T | ||
NM_016131.4:c.*151G>T | NP_057215.3:n.*151G>T | |
XM_024452565.1:c.*151G>T | XP_024308333.1:n.*151G>T | |
NM_016131.5:c.*151G>T MANE Select | NP_057215.3:n.*151G>T |