Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150977889C= , CM000669.2:g.150977889C= | GRCh38 |
| NC_000007.13:g.150674977C= , CM000669.1:g.150674977C= | GRCh37 |
| NC_000007.12:g.150305910C= | NCBI36 |
| NG_008916.1:g.5038G= , LRG_288:g.5038G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262186.10:c.25G= MANE Select | ENSP00000262186.5:p.Ala9= | |
| ENST00000262186.9:c.25G= | ENSP00000262186.5:p.Ala9= | |
| ENST00000430723.4:c.-153G= | ENSP00000387657.4:n.-153G= | |
| ENST00000532957.5:n.248G= | ||
| NM_000238.3:c.25G= , LRG_288t1:c.25G= | NP_000229.1:p.Ala9= | |
| NM_172056.2:c.25G= , LRG_288t2:c.25G= | NP_742053.1:p.Ala9= | |
| XM_011516186.1:c.25G= | XP_011514488.1:p.Ala9= | |
| XM_011516186.3:c.25G= | XP_011514488.1:p.Ala9= | |
| NM_000238.4:c.25G= MANE Select | NP_000229.1:p.Ala9= |