HGVS | Genome Assembly |
---|---|
NC_000019.10:g.33302026C= , CM000681.2:g.33302026C= | GRCh38 |
NC_000019.9:g.33792932C= , CM000681.1:g.33792932C= | GRCh37 |
NC_000019.8:g.38484772C= | NCBI36 |
NG_012022.1:g.5499G= , LRG_456:g.5499G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000498907.3:c.389G= MANE Select | ENSP00000427514.1:p.Gly130= | |
ENST00000498907.2:c.389G= | ENSP00000427514.1:p.Gly130= | |
NM_001285829.1:c.32G= | NP_001272758.1:p.Gly11= | |
NM_001287424.1:c.494G= | NP_001274353.1:p.Gly165= | |
NM_001287435.1:c.347G= | NP_001274364.1:p.Gly116= | |
NM_004364.4:c.389G= | NP_004355.2:p.Gly130= | |
NM_001287424.2:c.494G= | NP_001274353.1:p.Gly165= | |
NM_004364.5:c.389G= MANE Select | NP_004355.2:p.Gly130= | |
NM_001285829.2:c.32G= | NP_001272758.1:p.Gly11= | |
NM_001287435.2:c.347G= | NP_001274364.1:p.Gly116= |