HGVS | Genome Assembly |
---|---|
NC_000004.12:g.185144806A>C , CM000666.2:g.185144806A>C | GRCh38 |
NC_000004.11:g.186065960A>C , CM000666.1:g.186065960A>C | GRCh37 |
NC_000004.10:g.186302954A>C | NCBI36 |
NG_013001.1:g.6544A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000281456.11:c.154A>C MANE Select | ENSP00000281456.5:p.Lys52Gln | |
ENST00000281456.10:c.154A>C | ENSP00000281456.5:p.Lys52Gln | |
ENST00000491736.1:c.154A>C | ENSP00000476711.1:p.Lys52Gln | |
NM_001151.3:c.154A>C | NP_001142.2:p.Lys52Gln | |
NM_001151.4:c.154A>C MANE Select | NP_001142.2:p.Lys52Gln |