Canonical Allele Identifier: CA10654609

Gene:

Linked Data

• ClinVar Variation Id: 369312
• ClinVar RCV Id: RCV000348587 ; RCV000393280
• dbSNP Id: rs189308010
• gnomAD v2: 2-166248824-G-A
• gnomAD v3: 2-165392314-G-A
• gnomAD v4: 2-165392314-G-A
• MyVariant Identifiers: chr2:g.166248824G>A (hg19) ; chr2:g.165392314G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165392314G>A , CM000664.2:g.165392314G>A	GRCh38
NC_000002.11:g.166248824G>A , CM000664.1:g.166248824G>A	GRCh37
NC_000002.10:g.165957070G>A	NCBI36
NG_008143.1:g.157913G>A