HGVS | Genome Assembly |
---|---|
NC_000005.10:g.148827577A>C , CM000667.2:g.148827577A>C | GRCh38 |
NC_000005.9:g.148207140A>C , CM000667.1:g.148207140A>C | GRCh37 |
NC_000005.8:g.148187333A>C | NCBI36 |
NG_016421.1:g.5985A>C | |
NG_016421.2:g.5985A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000305988.6:c.746A>C MANE Select | ENSP00000305372.4:p.Glu249Ala | |
ENST00000305988.5:c.746A>C | ENSP00000305372.4:p.Glu249Ala | |
NM_000024.5:c.746A>C | NP_000015.1:p.Glu249Ala | |
NM_000024.6:c.746A>C MANE Select | NP_000015.2:p.Glu249Ala |