Canonical Allele Identifier: CA10654666

Gene:

Linked Data

• ClinVar Variation Id: 369424
• ClinVar RCV Id: RCV000316645
• dbSNP Id: rs10865561
• gnomAD v2: 3-77699129-C-T
• gnomAD v3: 3-77649978-C-T
• gnomAD v4: 3-77649978-C-T
• MyVariant Identifiers: chr3:g.77699129C>T (hg19) ; chr3:g.77649978C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.77649978C>T , CM000665.2:g.77649978C>T	GRCh38
NC_000003.11:g.77699129C>T , CM000665.1:g.77699129C>T	GRCh37
NC_000003.10:g.77781819C>T	NCBI36
NG_027734.1:g.1748285C>T
NG_027734.2:g.1748285C>T