Canonical Allele Identifier: CA11297605

Gene:

Linked Data

• ClinVar Variation Id: 16922
• ClinVar RCV Id: RCV001515646
• dbSNP Id: rs3087243
• gnomAD v2: 2-204738919-G-A
• gnomAD v3: 2-203874196-G-A
• gnomAD v4: 2-203874196-G-A
• MyVariant Identifiers: chr2:g.204738919G>A (hg19) ; chr2:g.203874196G>A (hg38)
• PubMed: PMID:12724780 ; PMID:15199380

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203874196G>A , CM000664.2:g.203874196G>A	GRCh38
NC_000002.11:g.204738919G>A , CM000664.1:g.204738919G>A	GRCh37
NC_000002.10:g.204447164G>A	NCBI36
NG_011502.1:g.11411G>A