Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.23868022A>T , CM000663.2:g.23868022A>T | GRCh38 |
| NC_000001.10:g.24194512A>T , CM000663.1:g.24194512A>T | GRCh37 |
| NC_000001.9:g.24067099A>T | NCBI36 |
| NG_013346.1:g.5348T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374479.4:c.265T>A MANE Select | ENSP00000363603.3:p.Tyr89Asn | |
| ENST00000374479.3:c.265T>A | ENSP00000363603.3:p.Tyr89Asn | |
| NM_000147.4:c.265T>A | NP_000138.2:p.Tyr89Asn | |
| XM_005245821.1:c.-285T>A | XP_005245878.1:n.-285T>A | |
| XM_005245821.3:c.-285T>A | XP_005245878.1:n.-285T>A | |
| NM_000147.5:c.265T>A MANE Select | NP_000138.2:p.Tyr89Asn | |
| NR_174379.1:n.269T>A | ||
| NR_174380.1:n.269T>A | ||
| NR_174381.1:n.269T>A | ||
| NR_174382.1:n.269T>A |