HGVS | Genome Assembly |
---|---|
NC_000013.11:g.110174376C= , CM000675.2:g.110174376C= | GRCh38 |
NC_000013.10:g.110826723C= , CM000675.1:g.110826723C= | GRCh37 |
NC_000013.9:g.109624724C= | NCBI36 |
NG_011544.2:g.137774G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000375820.10:c.3406+70G= MANE Select | ENSP00000364979.4:n.3406+70G= | |
ENST00000375820.8:c.3406+70G= | ENSP00000364979.4:n.3406+70G= | |
NM_001845.5:c.3406+70G= | NP_001836.3:n.3406+70G= | |
XM_011521048.1:c.3214+70G= | XP_011519350.1:n.3214+70G= | |
XM_011521048.2:c.3214+70G= | XP_011519350.1:n.3214+70G= | |
NM_001845.6:c.3406+70G= MANE Select | NP_001836.3:n.3406+70G= |