Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240877581T>G , CM000664.2:g.240877581T>G | GRCh38 |
| NC_000002.11:g.241816998T>G , CM000664.1:g.241816998T>G | GRCh37 |
| NC_000002.10:g.241465671T>G | NCBI36 |
| NG_008005.1:g.13837T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.891T>G MANE Select | ENSP00000302620.3:p.Tyr297Ter | |
| ENST00000307503.3:c.891T>G | ENSP00000302620.3:p.Tyr297Ter | |
| ENST00000470255.1:n.669T>G | ||
| NM_000030.2:c.891T>G | NP_000021.1:p.Tyr297Ter | |
| NM_000030.3:c.891T>G MANE Select | NP_000021.1:p.Tyr297Ter |