Canonical Allele Identifier: CA184586838

Gene:

Linked Data

• dbSNP Id: rs1023284198
• gnomAD v3: 8-123753566-C-T
• gnomAD v4: 8-123753566-C-T
• MyVariant Identifiers: chr8:g.124765806C>T (hg19) ; chr8:g.123753566C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.123753566C>T , CM000670.2:g.123753566C>T	GRCh38
NC_000008.10:g.124765806C>T , CM000670.1:g.124765806C>T	GRCh37
NC_000008.9:g.124834987C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_928607.1:n.153-11217C>T
XR_928607.3:n.324-11217C>T