Canonical Allele Identifier: CA11025144

Gene:

Linked Data

• ClinVar Variation Id: 869139
• ClinVar RCV Id: RCV001078163
• dbSNP Id: rs1143623
• gnomAD v2: 2-113595829-C-G
• gnomAD v3: 2-112838252-C-G
• gnomAD v4: 2-112838252-C-G
• MyVariant Identifiers: chr2:g.113595829C>G (hg19) ; chr2:g.112838252C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112838252C>G , CM000664.2:g.112838252C>G	GRCh38
NC_000002.11:g.113595829C>G , CM000664.1:g.113595829C>G	GRCh37
NC_000002.10:g.113312300C>G	NCBI36
NG_008851.1:g.3528G>C