HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17023934A>T , CM000663.2:g.17023934A>T | GRCh38 |
NC_000001.10:g.17350429A>T , CM000663.1:g.17350429A>T | GRCh37 |
NC_000001.9:g.17223016A>T | NCBI36 |
NG_012340.1:g.35237T>A , LRG_316:g.35237T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000463045.3:c.471+39T>A | ENSP00000481376.2:n.471+39T>A | |
ENST00000491274.6:c.600+39T>A | ENSP00000480482.2:n.600+39T>A | |
ENST00000375499.8:c.642+39T>A MANE Select | ENSP00000364649.3:n.642+39T>A | |
ENST00000375499.7:c.642+39T>A | ENSP00000364649.3:n.642+39T>A | |
ENST00000485515.5:n.576+39T>A | ||
NM_003000.2:c.642+39T>A , LRG_316t1:c.642+39T>A | NP_002991.2:n.642+39T>A | |
NM_003000.3:c.642+39T>A MANE Select | NP_002991.2:n.642+39T>A |