HGVS | Genome Assembly |
---|---|
NC_000002.12:g.46385492C>T , CM000664.2:g.46385492C>T | GRCh38 |
NC_000002.11:g.46612631C>T , CM000664.1:g.46612631C>T | GRCh37 |
NC_000002.10:g.46466135C>T | NCBI36 |
NG_016000.1:g.93091C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263734.5:c.*832C>T MANE Select | ENSP00000263734.3:n.*832C>T | |
ENST00000263734.4:c.*832C>T | ENSP00000263734.3:n.*832C>T | |
ENST00000466465.5:n.2418C>T | ||
NM_001430.4:c.*832C>T | NP_001421.2:n.*832C>T | |
XM_011532698.1:c.*832C>T | XP_011531000.1:n.*832C>T | |
XM_011532698.2:c.*832C>T | XP_011531000.1:n.*832C>T | |
NM_001430.5:c.*832C>T MANE Select | NP_001421.2:n.*832C>T |