HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133256093T= , CM000671.2:g.133256093T= | GRCh38 |
NC_000009.11:g.136131480T= , CM000671.1:g.136131480T= | GRCh37 |
NC_000009.10:g.135121301T= | NCBI36 |
NG_006669.1:g.21575A= | |
NG_006669.2:g.24123A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000453660.4:n.667A= | ||
ENST00000647353.1:n.54-4941A= | ||
ENST00000679909.1:c.28+19069A= | ENSP00000506089.1:n.28+19069A= | |
ENST00000453660.3:n.649A= | ||
ENST00000538324.2:c.635A= | ENSP00000483018.1:p.Asp212= | |
ENST00000611156.4:c.635A= | ENSP00000483265.1:p.Asp212= | |
NM_020469.2:c.638A= | NP_065202.2:p.Asp213= | |
NM_020469.3:c.638A= | NP_065202.2:p.Asp213= |