HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133256079C= , CM000671.2:g.133256079C= | GRCh38 |
NC_000009.11:g.136131466C= , CM000671.1:g.136131466C= | GRCh37 |
NC_000009.10:g.135121287C= | NCBI36 |
NG_006669.1:g.21589G= | |
NG_006669.2:g.24137G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000453660.4:n.681G= | ||
ENST00000647353.1:n.54-4927G= | ||
ENST00000679909.1:c.28+19083G= | ENSP00000506089.1:n.28+19083G= | |
ENST00000453660.3:n.663G= | ||
ENST00000538324.2:c.649G= | ENSP00000483018.1:p.Asp217= | |
ENST00000611156.4:c.649G= | ENSP00000483265.1:p.Asp217= | |
NM_020469.2:c.652G= | NP_065202.2:p.Asp218= | |
NM_020469.3:c.652G= | NP_065202.2:p.Asp218= |