Linked Data
gnomAD v4:
19-18789296-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18789296C>T , CM000681.2:g.18789296C>T | GRCh38 |
| NC_000019.9:g.18900105C>T , CM000681.1:g.18900105C>T | GRCh37 |
| NC_000019.8:g.18761105C>T | NCBI36 |
| NG_007070.1:g.7010G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222271.7:c.392G>A MANE Select | ENSP00000222271.2:p.Cys131Tyr | |
| ENST00000222271.6:c.392G>A | ENSP00000222271.2:p.Cys131Tyr | |
| ENST00000425807.1:c.391-404G>A | ENSP00000403792.1:n.391-404G>A | |
| ENST00000542601.6:c.293G>A | ENSP00000439156.2:p.Cys98Tyr | |
| NM_000095.2:c.392G>A | NP_000086.2:p.Cys131Tyr | |
| NM_000095.3:c.392G>A MANE Select | NP_000086.2:p.Cys131Tyr |