HGVS | Genome Assembly |
---|---|
NC_000012.12:g.4912300C>T , CM000674.2:g.4912300C>T | GRCh38 |
NC_000012.11:g.5021466C>T , CM000674.1:g.5021466C>T | GRCh37 |
NC_000012.10:g.4891727C>T | NCBI36 |
NG_011815.1:g.7394C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382545.5:c.922C>T MANE Select | ENSP00000371985.3:p.His308Tyr | |
ENST00000543874.3:n.105+1828C>T | ||
ENST00000639306.1:c.760C>T | ENSP00000492506.1:p.His254Tyr | |
ENST00000639680.1:c.76+34C>T | ||
ENST00000382545.3:c.922C>T | ENSP00000371985.3:p.His308Tyr | |
ENST00000541095.1:n.105+1828C>T | ||
ENST00000543874.2:n.96+1828C>T | ||
NM_000217.2:c.922C>T | NP_000208.2:p.His308Tyr | |
NM_000217.3:c.922C>T MANE Select | NP_000208.2:p.His308Tyr |