HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133274357T= , CM000671.2:g.133274357T= | GRCh38 |
NC_000009.11:g.136149773T= , CM000671.1:g.136149773T= | GRCh37 |
NC_000009.10:g.135139594T= | NCBI36 |
NG_006669.1:g.3277A= | |
NG_006669.2:g.5858A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000453660.4:n.58+805A= | ||
ENST00000647353.1:n.53+805A= | ||
ENST00000651471.1:n.63+1605A= | ||
ENST00000679909.1:c.28+805A= | ENSP00000506089.1:n.28+805A= | |
ENST00000453660.3:n.40+805A= | ||
ENST00000538324.2:c.28+805A= | ENSP00000483018.1:n.28+805A= | |
ENST00000611156.4:c.28+805A= | ENSP00000483265.1:n.28+805A= | |
NM_020469.2:c.28+805A= | NP_065202.2:n.28+805A= | |
NM_020469.3:c.28+805A= | NP_065202.2:n.28+805A= |