HGVS | Genome Assembly |
---|---|
NC_000011.10:g.66560343A>T , CM000673.2:g.66560343A>T | GRCh38 |
NC_000011.9:g.66327814A>T , CM000673.1:g.66327814A>T | GRCh37 |
NC_000011.8:g.66084390A>T | NCBI36 |
NG_013304.2:g.18424A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000513398.2:c.1677+32A>T MANE Select | ENSP00000426797.1:n.1677+32A>T | |
ENST00000502692.5:c.1806+32A>T | ENSP00000422007.1:n.1806+32A>T | |
ENST00000513398.1:c.1677+32A>T | ENSP00000426797.1:n.1677+32A>T | |
NM_001104.3:c.1677+32A>T | NP_001095.2:n.1677+32A>T | |
NM_001258371.2:c.1806+32A>T | NP_001245300.2:n.1806+32A>T | |
NM_001104.4:c.1677+32A>T MANE Select | NP_001095.2:n.1677+32A>T | |
NM_001258371.3:c.1806+32A>T | NP_001245300.2:n.1806+32A>T |