HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23431631G= , CM000676.2:g.23431631G= | GRCh38 |
NC_000014.8:g.23900840G= , CM000676.1:g.23900840G= | GRCh37 |
NC_000014.7:g.22970680G= | NCBI36 |
NG_007884.1:g.9031C= , LRG_384:g.9031C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.686C= MANE Select | ENSP00000347507.3:p.Ala229= | |
ENST00000355349.3:c.686C= | ENSP00000347507.3:p.Ala229= | |
NM_000257.3:c.686C= | NP_000248.2:p.Ala229= | |
XR_245686.3:n.792C= | ||
XM_017021340.1:c.686C= | XP_016876829.1:p.Ala229= | |
NM_000257.4:c.686C= MANE Select | NP_000248.2:p.Ala229= |