HGVS | Genome Assembly |
---|---|
NC_000019.10:g.33302025G= , CM000681.2:g.33302025G= | GRCh38 |
NC_000019.9:g.33792931G= , CM000681.1:g.33792931G= | GRCh37 |
NC_000019.8:g.38484771G= | NCBI36 |
NG_012022.1:g.5500C= , LRG_456:g.5500C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000498907.3:c.390C= MANE Select | ENSP00000427514.1:p.Gly130= | |
ENST00000498907.2:c.390C= | ENSP00000427514.1:p.Gly130= | |
NM_001285829.1:c.33C= | NP_001272758.1:p.Gly11= | |
NM_001287424.1:c.495C= | NP_001274353.1:p.Gly165= | |
NM_001287435.1:c.348C= | NP_001274364.1:p.Gly116= | |
NM_004364.4:c.390C= | NP_004355.2:p.Gly130= | |
NM_001287424.2:c.495C= | NP_001274353.1:p.Gly165= | |
NM_004364.5:c.390C= MANE Select | NP_004355.2:p.Gly130= | |
NM_001285829.2:c.33C= | NP_001272758.1:p.Gly11= | |
NM_001287435.2:c.348C= | NP_001274364.1:p.Gly116= |