HGVS | Genome Assembly |
---|---|
NC_000012.12:g.4912505G>T , CM000674.2:g.4912505G>T | GRCh38 |
NC_000012.11:g.5021671G>T , CM000674.1:g.5021671G>T | GRCh37 |
NC_000012.10:g.4891932G>T | NCBI36 |
NG_011815.1:g.7599G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382545.5:c.1127G>T MANE Select | ENSP00000371985.3:p.Gly376Val | |
ENST00000543874.3:n.105+2033G>T | ||
ENST00000639306.1:c.965G>T | ENSP00000492506.1:p.Gly322Val | |
ENST00000639680.1:c.76+239G>T | ||
ENST00000382545.3:c.1127G>T | ENSP00000371985.3:p.Gly376Val | |
ENST00000541095.1:n.105+2033G>T | ||
ENST00000543874.2:n.96+2033G>T | ||
NM_000217.2:c.1127G>T | NP_000208.2:p.Gly376Val | |
NM_000217.3:c.1127G>T MANE Select | NP_000208.2:p.Gly376Val |