HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133255863C= , CM000671.2:g.133255863C= | GRCh38 |
NC_000009.11:g.136131250C= , CM000671.1:g.136131250C= | GRCh37 |
NC_000009.10:g.135121071C= | NCBI36 |
NG_006669.1:g.21805G= | |
NG_006669.2:g.24353G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000453660.4:n.897G= | ||
ENST00000647353.1:n.54-4711G= | ||
ENST00000679909.1:c.28+19299G= | ENSP00000506089.1:n.28+19299G= | |
ENST00000453660.3:n.879G= | ||
ENST00000538324.2:c.865G= | ENSP00000483018.1:p.Val289= | |
ENST00000611156.4:c.865G= | ENSP00000483265.1:p.Val289= | |
NM_020469.2:c.868G= | NP_065202.2:p.Val290= | |
NM_020469.3:c.868G= | NP_065202.2:p.Val290= |