HGVS | Genome Assembly |
---|---|
NC_000006.12:g.6248384C= , CM000668.2:g.6248384C= | GRCh38 |
NC_000006.11:g.6248617C= , CM000668.1:g.6248617C= | GRCh37 |
NC_000006.10:g.6193616C= | NCBI36 |
NG_008107.1:g.77308G= , LRG_549:g.77308G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264870.8:c.726G= MANE Select | ENSP00000264870.3:p.Val242= | |
ENST00000264870.7:c.726G= | ENSP00000264870.3:p.Val242= | |
NM_000129.3:c.726G= , LRG_549t1:c.726G= | NP_000120.2:p.Val242= | |
XM_006715010.2:c.726G= | XP_006715073.1:p.Val242= | |
XM_011514342.1:c.888G= | XP_011512644.1:p.Val296= | |
NM_000129.4:c.726G= MANE Select | NP_000120.2:p.Val242= |