Canonical Allele Identifier:
CA11732018
Gene:
gnomAD v2:
gnomAD v3:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.111874141T>A , CM000666.2:g.111874141T>A | GRCh38 |
| NC_000004.11:g.112795297T>A , CM000666.1:g.112795297T>A | GRCh37 |
| NC_000004.10:g.113014746T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_939076.1:n.170+23835T>A | ||
| XR_939077.1:n.659+23835T>A | ||
| XR_939076.2:n.170+23835T>A | ||
| XR_939077.2:n.668+23835T>A |