HGVS | Genome Assembly |
---|---|
NC_000008.11:g.118110146C>A , CM000670.2:g.118110146C>A | GRCh38 |
NC_000008.10:g.119122385C>A , CM000670.1:g.119122385C>A | GRCh37 |
NC_000008.9:g.119191566C>A | NCBI36 |
NG_007455.2:g.6674G>T , LRG_493:g.6674G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000378204.7:c.901G>T MANE Select | ENSP00000367446.3:p.Gly301Cys | |
ENST00000436216.2:c.269G>T | ||
ENST00000378204.6:c.901G>T | ENSP00000367446.2:p.Gly301Cys | |
ENST00000436216.1:c.269G>T | ||
ENST00000437196.1:c.73+828G>T | ENSP00000407299.1:n.73+828G>T | |
NM_000127.2:c.901G>T , LRG_493t1:c.901G>T | NP_000118.2:p.Gly301Cys | |
NM_000127.3:c.901G>T MANE Select | NP_000118.2:p.Gly301Cys |