Linked Data
gnomAD v4:
22-32104649-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.32104649T>A , CM000684.2:g.32104649T>A | GRCh38 |
| NC_000022.10:g.32500636T>A , CM000684.1:g.32500636T>A | GRCh37 |
| NC_000022.9:g.30830636T>A | NCBI36 |
| NG_017045.1:g.66618T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266088.9:c.1666-137T>A MANE Select | ENSP00000266088.4:n.1666-137T>A | |
| ENST00000266088.8:c.1666-137T>A | ENSP00000266088.4:n.1666-137T>A | |
| ENST00000543737.2:c.1285-137T>A | ENSP00000444898.1:n.1285-137T>A | |
| NM_000343.3:c.1666-137T>A | NP_000334.1:n.1666-137T>A | |
| NM_001256314.1:c.1285-137T>A | NP_001243243.1:n.1285-137T>A | |
| XR_938173.1:n.591+2189A>T | ||
| XR_938174.1:n.486+15206A>T | ||
| NM_000343.4:c.1666-137T>A MANE Select | NP_000334.1:n.1666-137T>A | |
| NM_001256314.2:c.1285-137T>A | NP_001243243.1:n.1285-137T>A |