HGVS | Genome Assembly |
---|---|
NC_000010.11:g.30313944A>T , CM000672.2:g.30313944A>T | GRCh38 |
NC_000010.10:g.30602873A>T , CM000672.1:g.30602873A>T | GRCh37 |
NC_000010.9:g.30642879A>T | NCBI36 |
NG_028096.1:g.40395T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263063.9:c.1414T>A MANE Select | ENSP00000263063.3:p.Ser472Thr | |
ENST00000263063.8:c.1414T>A | ENSP00000263063.3:p.Ser472Thr | |
ENST00000488290.5:n.3169T>A | ||
NM_018109.3:c.1414T>A | NP_060579.3:p.Ser472Thr | |
NM_018109.4:c.1414T>A MANE Select | NP_060579.3:p.Ser472Thr |