HGVS | Genome Assembly |
---|---|
NC_000010.11:g.30313929G= , CM000672.2:g.30313929G= | GRCh38 |
NC_000010.10:g.30602858G= , CM000672.1:g.30602858G= | GRCh37 |
NC_000010.9:g.30642864G= | NCBI36 |
NG_028096.1:g.40410C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000263063.9:c.1429C= MANE Select | ENSP00000263063.3:p.Gln477= | |
ENST00000263063.8:c.1429C= | ENSP00000263063.3:p.Gln477= | |
ENST00000488290.5:n.3184C= | ||
NM_018109.3:c.1429C= | NP_060579.3:p.Gln477= | |
NM_018109.4:c.1429C= MANE Select | NP_060579.3:p.Gln477= |