Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.44310443C= , CM000667.2:g.44310443C= | GRCh38 |
| NC_000005.9:g.44310545C= , CM000667.1:g.44310545C= | GRCh37 |
| NC_000005.8:g.44346302C= | NCBI36 |
| NG_011446.1:g.83240G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004465.2:c.413G= MANE Select | NP_004456.1:p.Gly138= |
| ENST00000264664.5:c.413G= MANE Select | ENSP00000264664.4:p.Gly138= |
| NM_004465.1:c.413G= | NP_004456.1:p.Gly138= |
| ENST00000264664.4:c.413G= | ENSP00000264664.4:p.Gly138= |
| XM_005248264.2:c.413G= | XP_005248321.1:p.Gly138= |
| XM_005248264.4:c.413G= | XP_005248321.1:p.Gly138= |