Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18787628T>C , CM000681.2:g.18787628T>C | GRCh38 |
| NC_000019.9:g.18898437T>C , CM000681.1:g.18898437T>C | GRCh37 |
| NC_000019.8:g.18759437T>C | NCBI36 |
| NG_007070.1:g.8678A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222271.7:c.998A>G MANE Select | ENSP00000222271.2:p.Asn333Ser | |
| ENST00000222271.6:c.998A>G | ENSP00000222271.2:p.Asn333Ser | |
| ENST00000425807.1:c.839A>G | ENSP00000403792.1:p.Asn280Ser | |
| ENST00000542601.6:c.899A>G | ENSP00000439156.2:p.Asn300Ser | |
| NM_000095.2:c.998A>G | NP_000086.2:p.Asn333Ser | |
| NM_000095.3:c.998A>G MANE Select | NP_000086.2:p.Asn333Ser |