HGVS | Genome Assembly |
---|---|
NC_000017.11:g.70175863A>C , CM000679.2:g.70175863A>C | GRCh38 |
NC_000017.10:g.68172004A>C , CM000679.1:g.68172004A>C | GRCh37 |
NC_000017.9:g.65683599A>C | NCBI36 |
NG_008798.1:g.11329A>C , LRG_328:g.11329A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000243457.4:c.824A>C MANE Select | ENSP00000243457.2:p.Glu275Ala | |
ENST00000243457.3:c.824A>C | ENSP00000243457.2:p.Glu275Ala | |
ENST00000535240.1:c.824A>C | ENSP00000441848.1:p.Glu275Ala | |
NM_000891.2:c.824A>C , LRG_328t1:c.824A>C | NP_000882.1:p.Glu275Ala | |
XM_011524779.1:c.824A>C | XP_011523081.1:p.Glu275Ala | |
NM_000891.3:c.824A>C MANE Select | NP_000882.1:p.Glu275Ala |