HGVS | Genome Assembly |
---|---|
NC_000001.11:g.11965481A>C , CM000663.2:g.11965481A>C | GRCh38 |
NC_000001.10:g.12025538A>C , CM000663.1:g.12025538A>C | GRCh37 |
NC_000001.9:g.11948125A>C | NCBI36 |
NG_008159.1:g.35793A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000196061.5:c.1472A>C MANE Select | ENSP00000196061.4:p.Asp491Ala | |
ENST00000196061.4:c.1472A>C | ENSP00000196061.4:p.Asp491Ala | |
ENST00000470133.1:n.86A>C | ||
ENST00000491536.5:n.100A>C | ||
NM_000302.3:c.1472A>C | NP_000293.2:p.Asp491Ala | |
NM_001316320.1:c.1613A>C | NP_001303249.1:p.Asp538Ala | |
XM_011541594.1:c.1553A>C | XP_011539896.1:p.Asp518Ala | |
XM_024447707.1:c.806A>C | XP_024303475.1:p.Asp269Ala | |
NM_000302.4:c.1472A>C MANE Select | NP_000293.2:p.Asp491Ala | |
NM_001316320.2:c.1613A>C | NP_001303249.1:p.Asp538Ala |