HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133255412A= , CM000671.2:g.133255412A= | GRCh38 |
NC_000009.11:g.136130799A= , CM000671.1:g.136130799A= | GRCh37 |
NC_000009.10:g.135120620A= | NCBI36 |
NG_006669.1:g.22256T= | |
NG_006669.2:g.24804T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000453660.4:n.1348T= | ||
ENST00000647353.1:n.54-4260T= | ||
ENST00000679909.1:c.28+19750T= | ENSP00000506089.1:n.28+19750T= | |
ENST00000453660.3:n.1330T= | ||
ENST00000611156.4:c.*254T= | ENSP00000483265.1:n.*254T= | |
NM_020469.2:c.*254T= | NP_065202.2:n.*254T= | |
NM_020469.3:c.*254T= | NP_065202.2:n.*254T= |