HGVS | Genome Assembly |
---|---|
NC_000008.11:g.24952655C>T , CM000670.2:g.24952655C>T | GRCh38 |
NC_000008.10:g.24810168C>T , CM000670.1:g.24810168C>T | GRCh37 |
NC_000008.9:g.24866085C>T | NCBI36 |
NG_008492.1:g.8963G>A , LRG_259:g.8963G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000610854.2:c.*155G>A MANE Select | ENSP00000482169.2:n.*155G>A | |
ENST00000610854.1:c.*155G>A | ENSP00000482169.1:n.*155G>A | |
ENST00000619417.1:c.*652G>A | ENSP00000483690.1:n.*652G>A | |
NM_006158.4:c.*155G>A , LRG_259t1:c.*155G>A | NP_006149.2:n.*155G>A | |
NM_006158.5:c.*155G>A MANE Select | NP_006149.2:n.*155G>A |