HGVS | Genome Assembly |
---|---|
NC_000009.12:g.128945772C= , CM000671.2:g.128945772C= | GRCh38 |
NC_000009.11:g.131708051C= , CM000671.1:g.131708051C= | GRCh37 |
NC_000009.10:g.130747872C= | NCBI36 |
NG_017009.1:g.6962G= , LRG_744:g.6962G= | |
NG_033111.1:g.3080C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372586.4:c.1532G= MANE Select | ENSP00000361667.3:p.Ser511= | |
ENST00000372586.3:c.1532G= | ENSP00000361667.3:p.Ser511= | |
ENST00000482796.1:c.39-3417C= | ENSP00000417556.2:n.39-3417C= | |
NM_014908.3:c.1532G= , LRG_744t1:c.1532G= | NP_055723.1:p.Ser511= | |
NM_014908.4:c.1532G= MANE Select | NP_055723.1:p.Ser511= |