Canonical Allele Identifier:
CA92863827
Gene:
gnomAD v3:
gnomAD v4:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.11628425T>A , CM000666.2:g.11628425T>A | GRCh38 |
| NC_000004.11:g.11630049T>A , CM000666.1:g.11630049T>A | GRCh37 |
| NC_000004.10:g.11239147T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001741361.1:n.1026+76471T>A |