HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133256101C>A , CM000671.2:g.133256101C>A | GRCh38 |
NC_000009.11:g.136131488C>A , CM000671.1:g.136131488C>A | GRCh37 |
NC_000009.10:g.135121309C>A | NCBI36 |
NG_006669.1:g.21567G>T | |
NG_006669.2:g.24115G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000453660.4:n.659G>T | ||
ENST00000647353.1:n.54-4949G>T | ||
ENST00000679909.1:c.28+19061G>T | ENSP00000506089.1:n.28+19061G>T | |
ENST00000453660.3:n.641G>T | ||
ENST00000538324.2:c.627G>T | ENSP00000483018.1:p.Val209= | |
ENST00000611156.4:c.627G>T | ENSP00000483265.1:p.Val209= | |
NM_020469.2:c.630G>T | NP_065202.2:p.Val210= | |
NM_020469.3:c.630G>T | NP_065202.2:p.Val210= |