Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.4816815G= , CM000681.2:g.4816815G= | GRCh38 |
| NC_000019.9:g.4816827G= , CM000681.1:g.4816827G= | GRCh37 |
| NC_000019.8:g.4767827G= | NCBI36 |
| NG_031998.1:g.19928C= , LRG_358:g.19928C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248244.6:c.1563C= MANE Select | ENSP00000248244.4:p.Ala521= | |
| ENST00000248244.5:c.1563C= | ENSP00000248244.4:p.Ala521= | |
| ENST00000621756.1:c.1146C= | ENSP00000479467.1:p.Ala382= | |
| NM_182919.3:c.1563C= , LRG_358t1:c.1563C= | NP_891549.1:p.Ala521= | |
| NM_001385678.1:c.1521C= | NP_001372607.1:p.Ala507= | |
| NM_001385679.1:c.1428C= | NP_001372608.1:p.Ala476= | |
| NM_001385680.1:c.921C= | NP_001372609.1:p.Ala307= | |
| NM_182919.4:c.1563C= MANE Select | NP_891549.1:p.Ala521= |