HGVS | Genome Assembly |
---|---|
NC_000001.11:g.154576077C= , CM000663.2:g.154576077C= | GRCh38 |
NC_000001.10:g.154548553C= , CM000663.1:g.154548553C= | GRCh37 |
NC_000001.9:g.152815177C= | NCBI36 |
NG_008027.1:g.13297C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000368476.4:c.*145C= MANE Select | ENSP00000357461.3:n.*145C= | |
ENST00000636034.1:c.1505+149C= | ENSP00000489703.1:n.1505+149C= | |
ENST00000637900.1:c.*145C= | ENSP00000490474.1:n.*145C= | |
ENST00000368476.3:c.*145C= | ENSP00000357461.3:n.*145C= | |
NM_000748.2:c.*145C= | NP_000739.1:n.*145C= | |
XM_017000180.2:c.*145C= | XP_016855669.1:n.*145C= | |
XR_001736952.2:n.1906C= | ||
NM_000748.3:c.*145C= MANE Select | NP_000739.1:n.*145C= |