Linked Data
gnomAD v4:
11-17553446-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.17553446A>G , CM000673.2:g.17553446A>G | GRCh38 |
| NC_000011.9:g.17574993A>G , CM000673.1:g.17574993A>G | GRCh37 |
| NC_000011.8:g.17531569A>G | NCBI36 |
| NG_033191.1:g.11074A>G | |
| NG_033191.2:g.11074A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000399391.7:c.503A>G | ENSP00000382323.2:p.Tyr168Cys | |
| ENST00000399397.6:c.467A>G MANE Select | ENSP00000382329.2:p.Tyr156Cys | |
| ENST00000399391.6:c.503A>G | ENSP00000382323.2:p.Tyr168Cys | |
| ENST00000399397.5:c.467A>G | ENSP00000382329.2:p.Tyr156Cys | |
| ENST00000498332.5:n.373A>G | ||
| NM_001277269.1:c.503A>G | NP_001264198.1:p.Tyr168Cys | |
| NM_001292063.1:c.467A>G | NP_001278992.1:p.Tyr156Cys | |
| NM_001277269.2:c.503A>G | NP_001264198.1:p.Tyr168Cys | |
| NM_001292063.2:c.467A>G MANE Select | NP_001278992.1:p.Tyr156Cys |