Canonical Allele Identifier:
CA2610262421
Gene:
Linked Data
gnomAD v4:
10-94762592-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94762592A>T , CM000672.2:g.94762592A>T | GRCh38 |
| NC_000010.10:g.96522349A>T , CM000672.1:g.96522349A>T | GRCh37 |
| NC_000010.9:g.96512339A>T | NCBI36 |
| NG_008384.2:g.4887A>T | |
| NG_008384.3:g.4912A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000464755.1:c.932-12466A>T | ENSP00000483243.1:n.932-12466A>T |