HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133255945A= , CM000671.2:g.133255945A= | GRCh38 |
NC_000009.11:g.136131332A= , CM000671.1:g.136131332A= | GRCh37 |
NC_000009.10:g.135121153A= | NCBI36 |
NG_006669.1:g.21723T= | |
NG_006669.2:g.24271T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000453660.4:n.815T= | ||
ENST00000647353.1:n.54-4793T= | ||
ENST00000679909.1:c.28+19217T= | ENSP00000506089.1:n.28+19217T= | |
ENST00000453660.3:n.797T= | ||
ENST00000538324.2:c.783T= | ENSP00000483018.1:p.Asp261= | |
ENST00000611156.4:c.783T= | ENSP00000483265.1:p.Asp261= | |
NM_020469.2:c.786T= | NP_065202.2:p.Asp262= | |
NM_020469.3:c.786T= | NP_065202.2:p.Asp262= |