HGVS | Genome Assembly |
---|---|
NC_000004.12:g.177442250T= , CM000666.2:g.177442250T= | GRCh38 |
NC_000004.11:g.178363404T= , CM000666.1:g.178363404T= | GRCh37 |
NC_000004.10:g.178600398T= | NCBI36 |
NG_011845.2:g.5254A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264595.7:c.126A= MANE Select | ENSP00000264595.2:p.Ala42= | |
ENST00000264595.6:c.126A= | ENSP00000264595.2:p.Ala42= | |
ENST00000506853.5:n.160A= | ||
ENST00000510955.5:n.160A= | ||
ENST00000511231.1:n.160A= | ||
NM_000027.3:c.126A= | NP_000018.2:p.Ala42= | |
NM_001171988.1:c.126A= | NP_001165459.1:p.Ala42= | |
NR_033655.1:n.254A= | ||
XM_006714123.2:c.126A= | XP_006714186.1:p.Ala42= | |
XR_001741155.2:n.220A= | ||
NM_000027.4:c.126A= MANE Select | NP_000018.2:p.Ala42= | |
NM_001171988.2:c.126A= | NP_001165459.1:p.Ala42= | |
NR_033655.2:n.188A= |