HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94780510G>T , CM000672.2:g.94780510G>T | GRCh38 |
NC_000010.10:g.96540267G>T , CM000672.1:g.96540267G>T | GRCh37 |
NC_000010.9:g.96530257G>T | NCBI36 |
NG_008384.2:g.22805G>T | |
NG_008384.3:g.22830G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371321.9:c.493G>T MANE Select | ENSP00000360372.3:p.Asp165Tyr | |
ENST00000645461.1:n.1546G>T | ||
ENST00000371321.7:c.493G>T | ENSP00000360372.3:p.Asp165Tyr | |
ENST00000464755.1:c.1256G>T | ENSP00000483243.1:n.1256G>T | |
NM_000769.2:c.493G>T | NP_000760.1:p.Asp165Tyr | |
NM_000769.4:c.493G>T MANE Select | NP_000760.1:p.Asp165Tyr |