HGVS | Genome Assembly |
---|---|
NC_000008.11:g.117837147A>T , CM000670.2:g.117837147A>T | GRCh38 |
NC_000008.10:g.118849386A>T , CM000670.1:g.118849386A>T | GRCh37 |
NC_000008.9:g.118918567A>T | NCBI36 |
NG_007455.2:g.279673T>A , LRG_493:g.279673T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000684189.1:n.484T>A | ||
ENST00000378204.7:c.1017T>A MANE Select | ENSP00000367446.3:p.Gly339= | |
ENST00000436216.2:c.385T>A | ||
ENST00000378204.6:c.1017T>A | ENSP00000367446.2:p.Gly339= | |
ENST00000436216.1:c.385T>A | ||
ENST00000437196.1:c.74-1596T>A | ENSP00000407299.1:n.74-1596T>A | |
NM_000127.2:c.1017T>A , LRG_493t1:c.1017T>A | NP_000118.2:p.Gly339= | |
NM_000127.3:c.1017T>A MANE Select | NP_000118.2:p.Gly339= |