HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159329165T>A , CM000667.2:g.159329165T>A | GRCh38 |
NC_000005.9:g.158756173T>A , CM000667.1:g.158756173T>A | GRCh37 |
NC_000005.8:g.158688751T>A | NCBI36 |
NG_009618.1:g.6309A>T , LRG_71:g.6309A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696750.1:c.-149+1267A>T | ENSP00000512849.1:n.-149+1267A>T | |
ENST00000696751.1:c.-1+1267A>T | ENSP00000512850.1:n.-1+1267A>T | |
ENST00000696752.1:n.432+1267A>T | ||
ENST00000231228.3:c.-1+1267A>T MANE Select | ENSP00000231228.2:n.-1+1267A>T | |
ENST00000231228.2:c.-1+1267A>T | ENSP00000231228.2:n.-1+1267A>T | |
NM_002187.2:c.-1+1267A>T , LRG_71t1:c.-1+1267A>T | NP_002178.2:n.-1+1267A>T | |
NM_002187.3:c.-1+1267A>T MANE Select | NP_002178.2:n.-1+1267A>T |