Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18786033T>A , CM000681.2:g.18786033T>A | GRCh38 |
| NC_000019.9:g.18896843T>A , CM000681.1:g.18896843T>A | GRCh37 |
| NC_000019.8:g.18757843T>A | NCBI36 |
| NG_007070.1:g.10272A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222271.7:c.1421A>T MANE Select | ENSP00000222271.2:p.Asn474Ile | |
| ENST00000222271.6:c.1421A>T | ENSP00000222271.2:p.Asn474Ile | |
| ENST00000425807.1:c.1262A>T | ENSP00000403792.1:p.Asn421Ile | |
| ENST00000542601.6:c.1322A>T | ENSP00000439156.2:p.Asn441Ile | |
| NM_000095.2:c.1421A>T | NP_000086.2:p.Asn474Ile | |
| NM_000095.3:c.1421A>T MANE Select | NP_000086.2:p.Asn474Ile |