Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.4816639T= , CM000681.2:g.4816639T= | GRCh38 |
| NC_000019.9:g.4816651T= , CM000681.1:g.4816651T= | GRCh37 |
| NC_000019.8:g.4767651T= | NCBI36 |
| NG_031998.1:g.20104A= , LRG_358:g.20104A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248244.6:c.1739A= MANE Select | ENSP00000248244.4:p.Tyr580= | |
| ENST00000248244.5:c.1739A= | ENSP00000248244.4:p.Tyr580= | |
| ENST00000621756.1:c.1322A= | ENSP00000479467.1:p.Tyr441= | |
| NM_182919.3:c.1739A= , LRG_358t1:c.1739A= | NP_891549.1:p.Tyr580= | |
| NM_001385678.1:c.1697A= | NP_001372607.1:p.Tyr566= | |
| NM_001385679.1:c.1604A= | NP_001372608.1:p.Tyr535= | |
| NM_001385680.1:c.1097A= | NP_001372609.1:p.Tyr366= | |
| NM_182919.4:c.1739A= MANE Select | NP_891549.1:p.Tyr580= |