Canonical Allele Identifier: CA545410442

Gene:

Linked Data

• dbSNP Id: rs1430154535
• gnomAD v2: 3-109462392-A-C
• gnomAD v3: 3-109743545-A-C
• gnomAD v4: 3-109743545-A-C
• MyVariant Identifiers: chr3:g.109462392A>C (hg19) ; chr3:g.109743545A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.109743545A>C , CM000665.2:g.109743545A>C	GRCh38
NC_000003.11:g.109462392A>C , CM000665.1:g.109462392A>C	GRCh37
NC_000003.10:g.110945082A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924325.1:n.142+63350A>C