HGVS | Genome Assembly |
---|---|
NC_000008.11:g.117836959A>T , CM000670.2:g.117836959A>T | GRCh38 |
NC_000008.10:g.118849198A>T , CM000670.1:g.118849198A>T | GRCh37 |
NC_000008.9:g.118918379A>T | NCBI36 |
NG_007455.2:g.279861T>A , LRG_493:g.279861T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684189.1:n.523+149T>A | ||
ENST00000378204.7:c.1056+149T>A MANE Select | ENSP00000367446.3:n.1056+149T>A | |
ENST00000436216.2:c.424+149T>A | ||
ENST00000378204.6:c.1056+149T>A | ENSP00000367446.2:n.1056+149T>A | |
ENST00000436216.1:c.424+149T>A | ||
ENST00000437196.1:c.74-1408T>A | ENSP00000407299.1:n.74-1408T>A | |
NM_000127.2:c.1056+149T>A , LRG_493t1:c.1056+149T>A | NP_000118.2:n.1056+149T>A | |
NM_000127.3:c.1056+149T>A MANE Select | NP_000118.2:n.1056+149T>A |