Canonical Allele Identifier: CA202788785
Gene:

Linked Data

dbSNP Id: rs930742504
gnomAD v2: 10-8739528-C-G
gnomAD v3: 10-8697565-C-G
gnomAD v4: 10-8697565-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8697565C>G , CM000672.2:g.8697565C>G GRCh38
NC_000010.10:g.8739528C>G , CM000672.1:g.8739528C>G GRCh37
NC_000010.9:g.8779534C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930641.1:n.33-27764G>C