Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18787613T>C , CM000681.2:g.18787613T>C | GRCh38 |
| NC_000019.9:g.18898422T>C , CM000681.1:g.18898422T>C | GRCh37 |
| NC_000019.8:g.18759422T>C | NCBI36 |
| NG_007070.1:g.8693A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222271.7:c.1013A>G MANE Select | ENSP00000222271.2:p.Asn338Ser | |
| ENST00000222271.6:c.1013A>G | ENSP00000222271.2:p.Asn338Ser | |
| ENST00000425807.1:c.854A>G | ENSP00000403792.1:p.Asn285Ser | |
| ENST00000542601.6:c.914A>G | ENSP00000439156.2:p.Asn305Ser | |
| NM_000095.2:c.1013A>G | NP_000086.2:p.Asn338Ser | |
| NM_000095.3:c.1013A>G MANE Select | NP_000086.2:p.Asn338Ser |