Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.4816569A>C , CM000681.2:g.4816569A>C | GRCh38 |
| NC_000019.9:g.4816581A>C , CM000681.1:g.4816581A>C | GRCh37 |
| NC_000019.8:g.4767581A>C | NCBI36 |
| NG_031998.1:g.20174T>G , LRG_358:g.20174T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248244.6:c.1809T>G MANE Select | ENSP00000248244.4:p.Tyr603Ter | |
| ENST00000248244.5:c.1809T>G | ENSP00000248244.4:p.Tyr603Ter | |
| ENST00000621756.1:c.1392T>G | ENSP00000479467.1:p.Tyr464Ter | |
| NM_182919.3:c.1809T>G , LRG_358t1:c.1809T>G | NP_891549.1:p.Tyr603Ter | |
| NM_001385678.1:c.1767T>G | NP_001372607.1:p.Tyr589Ter | |
| NM_001385679.1:c.1674T>G | NP_001372608.1:p.Tyr558Ter | |
| NM_001385680.1:c.1167T>G | NP_001372609.1:p.Tyr389Ter | |
| NM_182919.4:c.1809T>G MANE Select | NP_891549.1:p.Tyr603Ter |