HGVS | Genome Assembly |
---|---|
NC_000004.12:g.177440404T= , CM000666.2:g.177440404T= | GRCh38 |
NC_000004.11:g.178361558T= , CM000666.1:g.178361558T= | GRCh37 |
NC_000004.10:g.178598552T= | NCBI36 |
NG_011845.2:g.7100A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264595.7:c.150A= MANE Select | ENSP00000264595.2:p.Gly50= | |
ENST00000264595.6:c.150A= | ENSP00000264595.2:p.Gly50= | |
ENST00000506853.5:n.184A= | ||
ENST00000510955.5:n.184A= | ||
ENST00000511231.1:n.184A= | ||
NM_000027.3:c.150A= | NP_000018.2:p.Gly50= | |
NM_001171988.1:c.150A= | NP_001165459.1:p.Gly50= | |
NR_033655.1:n.278A= | ||
XM_006714123.2:c.150A= | XP_006714186.1:p.Gly50= | |
XR_001741155.2:n.244A= | ||
NM_000027.4:c.150A= MANE Select | NP_000018.2:p.Gly50= | |
NM_001171988.2:c.150A= | NP_001165459.1:p.Gly50= | |
NR_033655.2:n.212A= |