HGVS | Genome Assembly |
---|---|
NC_000023.11:g.48528295A= , CM000685.2:g.48528295A= | GRCh38 |
NC_000023.10:g.48386683A= , CM000685.1:g.48386683A= | GRCh37 |
NC_000023.9:g.48271627A= | NCBI36 |
NG_007452.1:g.11520A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000495186.6:c.531A= MANE Select | ENSP00000417052.1:p.Gly177= | |
ENST00000651615.1:c.469+1010A= | ENSP00000498524.1:n.469+1010A= | |
ENST00000276096.10:n.489A= | ||
ENST00000495186.5:c.531A= | ENSP00000417052.1:p.Gly177= | |
ENST00000498425.1:n.652A= | ||
NM_006579.2:c.531A= | NP_006570.1:p.Gly177= | |
NM_006579.3:c.531A= MANE Select | NP_006570.1:p.Gly177= |