HGVS | Genome Assembly |
---|---|
NC_000012.12:g.4912641G>T , CM000674.2:g.4912641G>T | GRCh38 |
NC_000012.11:g.5021807G>T , CM000674.1:g.5021807G>T | GRCh37 |
NC_000012.10:g.4892068G>T | NCBI36 |
NG_011815.1:g.7735G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382545.5:c.1263G>T MANE Select | ENSP00000371985.3:p.Gly421= | |
ENST00000543874.3:n.105+2169G>T | ||
ENST00000639306.1:c.1101G>T | ENSP00000492506.1:p.Gly367= | |
ENST00000639680.1:c.76+375G>T | ||
ENST00000382545.3:c.1263G>T | ENSP00000371985.3:p.Gly421= | |
ENST00000541095.1:n.105+2169G>T | ||
ENST00000543874.2:n.96+2169G>T | ||
NM_000217.2:c.1263G>T | NP_000208.2:p.Gly421= | |
NM_000217.3:c.1263G>T MANE Select | NP_000208.2:p.Gly421= |