Canonical Allele Identifier: CA1052103994

Gene:

Linked Data

• dbSNP Id: rs1708399842
• gnomAD v3: 3-109743423-A-C
• gnomAD v4: 3-109743423-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.109743423A>C , CM000665.2:g.109743423A>C	GRCh38
NC_000003.11:g.109462270A>C , CM000665.1:g.109462270A>C	GRCh37
NC_000003.10:g.110944960A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924325.1:n.142+63228A>C