Canonical Allele Identifier:
CA2610262415
Gene:
Linked Data
gnomAD v4:
10-94762588-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94762588G>T , CM000672.2:g.94762588G>T | GRCh38 |
| NC_000010.10:g.96522345G>T , CM000672.1:g.96522345G>T | GRCh37 |
| NC_000010.9:g.96512335G>T | NCBI36 |
| NG_008384.2:g.4883G>T | |
| NG_008384.3:g.4908G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000464755.1:c.932-12470G>T | ENSP00000483243.1:n.932-12470G>T |