HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159320411C>T , CM000667.2:g.159320411C>T | GRCh38 |
NC_000005.9:g.158747419C>T , CM000667.1:g.158747419C>T | GRCh37 |
NC_000005.8:g.158679997C>T | NCBI36 |
NG_009618.1:g.15063G>A , LRG_71:g.15063G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696750.1:c.-39G>A | ENSP00000512849.1:n.-39G>A | |
ENST00000696751.1:c.*87G>A | ENSP00000512850.1:n.*87G>A | |
ENST00000231228.3:c.592G>A MANE Select | ENSP00000231228.2:p.Ala198Thr | |
ENST00000231228.2:c.592G>A | ENSP00000231228.2:p.Ala198Thr | |
NM_002187.2:c.592G>A , LRG_71t1:c.592G>A | NP_002178.2:p.Ala198Thr | |
NM_002187.3:c.592G>A MANE Select | NP_002178.2:p.Ala198Thr |