Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.107695940G= , CM000669.2:g.107695940G= | GRCh38 |
| NC_000007.13:g.107336385G= , CM000669.1:g.107336385G= | GRCh37 |
| NC_000007.12:g.107123621G= | NCBI36 |
| NG_008489.1:g.40306G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000644269.2:c.1445G= MANE Select | ENSP00000494017.1:p.Trp482= | |
| ENST00000644846.1:c.156G= | ||
| ENST00000265715.7:c.1445G= | ENSP00000265715.3:p.Trp482= | |
| ENST00000460748.1:n.548G= | ||
| ENST00000477350.5:n.292G= | ||
| ENST00000480841.5:n.294G= | ||
| ENST00000497446.5:n.460G= | ||
| NM_000441.1:c.1445G= | NP_000432.1:p.Trp482= | |
| XM_005250425.1:c.1445G= | XP_005250482.1:p.Trp482= | |
| XM_005250425.2:c.1445G= | XP_005250482.1:p.Trp482= | |
| XM_017012318.1:c.1367G= | XP_016867807.1:p.Trp456= | |
| NM_000441.2:c.1445G= MANE Select | NP_000432.1:p.Trp482= |