Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.190402391G= , CM000665.2:g.190402391G= | GRCh38 |
| NC_000003.11:g.190120180G= , CM000665.1:g.190120180G= | GRCh37 |
| NC_000003.10:g.191602874G= | NCBI36 |
| NG_008149.1:g.19340G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264734.3:c.169G= MANE Select | ENSP00000264734.3:p.Gly57= | |
| ENST00000456423.2:c.115-7512G= | ENSP00000414136.2:n.115-7512G= | |
| ENST00000264734.2:c.379G= | ENSP00000264734.2:p.Gly127= | |
| ENST00000456423.1:c.325-7512G= | ENSP00000414136.1:n.325-7512G= | |
| ENST00000468220.1:n.361G= | ||
| NM_006580.3:c.379G= | NP_006571.1:p.Gly127= | |
| NM_001378492.1:c.169G= | NP_001365421.1:p.Gly57= | |
| NM_001378493.1:c.169G= | NP_001365422.1:p.Gly57= | |
| NM_006580.4:c.169G= MANE Select | NP_006571.2:p.Gly57= |