Canonical Allele Identifier:
CA1059429972
Gene:
gnomAD v3:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.12578159C>T , CM000666.2:g.12578159C>T | GRCh38 |
| NC_000004.11:g.12579783C>T , CM000666.1:g.12579783C>T | GRCh37 |
| NC_000004.10:g.12188881C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_925406.1:n.106+31183G>A | ||
| XR_001741374.1:n.254+44496G>A | ||
| XR_925406.3:n.140+31183G>A |