HGVS | Genome Assembly |
---|---|
NC_000002.12:g.219060423G= , CM000664.2:g.219060423G= | GRCh38 |
NC_000002.11:g.219925145G= , CM000664.1:g.219925145G= | GRCh37 |
NC_000002.10:g.219633389G= | NCBI36 |
NG_016741.1:g.5094C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295731.7:c.45C= MANE Select | ENSP00000295731.5:p.Val15= | |
ENST00000295731.6:c.45C= | ENSP00000295731.5:p.Val15= | |
NM_002181.3:c.45C= | NP_002172.2:p.Val15= | |
NM_002181.4:c.45C= MANE Select | NP_002172.2:p.Val15= |