Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.86030266T>C , CM000664.2:g.86030266T>C | GRCh38 |
| NC_000002.11:g.86257389T>C , CM000664.1:g.86257389T>C | GRCh37 |
| NC_000002.10:g.86110900T>C | NCBI36 |
| NG_050742.2:g.80890A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263857.11:c.4709A>G MANE Select | ENSP00000263857.6:p.Asn1570Ser | |
| ENST00000263857.10:c.4709A>G | ENSP00000263857.6:p.Asn1570Ser | |
| ENST00000409681.1:c.4526A>G | ENSP00000386300.1:p.Asn1509Ser | |
| NM_015425.3:c.4709A>G | NP_056240.2:p.Asn1570Ser | |
| XM_006711983.2:c.4385A>G | XP_006712046.1:p.Asn1462Ser | |
| NM_015425.5:c.4709A>G | NP_056240.2:p.Asn1570Ser | |
| NM_015425.6:c.4709A>G MANE Select | NP_056240.2:p.Asn1570Ser |