Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.4816569A= , CM000681.2:g.4816569A= | GRCh38 |
| NC_000019.9:g.4816581A= , CM000681.1:g.4816581A= | GRCh37 |
| NC_000019.8:g.4767581A= | NCBI36 |
| NG_031998.1:g.20174T= , LRG_358:g.20174T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248244.6:c.1809T= MANE Select | ENSP00000248244.4:p.Tyr603= | |
| ENST00000248244.5:c.1809T= | ENSP00000248244.4:p.Tyr603= | |
| ENST00000621756.1:c.1392T= | ENSP00000479467.1:p.Tyr464= | |
| NM_182919.3:c.1809T= , LRG_358t1:c.1809T= | NP_891549.1:p.Tyr603= | |
| NM_001385678.1:c.1767T= | NP_001372607.1:p.Tyr589= | |
| NM_001385679.1:c.1674T= | NP_001372608.1:p.Tyr558= | |
| NM_001385680.1:c.1167T= | NP_001372609.1:p.Tyr389= | |
| NM_182919.4:c.1809T= MANE Select | NP_891549.1:p.Tyr603= |