HGVS | Genome Assembly |
---|---|
NC_000010.11:g.110582033A>T , CM000672.2:g.110582033A>T | GRCh38 |
NC_000010.10:g.112341791A>T , CM000672.1:g.112341791A>T | GRCh37 |
NC_000010.9:g.112331781A>T | NCBI36 |
NG_012217.1:g.19343A>T , LRG_774:g.19343A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684988.1:n.791A>T | ||
ENST00000687823.1:n.572A>T | ||
ENST00000689932.1:n.2721A>T | ||
ENST00000691297.1:n.791A>T | ||
ENST00000691527.1:n.1461A>T | ||
ENST00000692792.1:n.777A>T | ||
ENST00000361804.5:c.658A>T MANE Select | ENSP00000354720.5:p.Arg220Ter | |
ENST00000361804.4:c.658A>T | ENSP00000354720.4:p.Arg220Ter | |
NM_005445.3:c.658A>T , LRG_774t1:c.658A>T | NP_005436.1:p.Arg220Ter | |
NM_005445.4:c.658A>T MANE Select | NP_005436.1:p.Arg220Ter |