Canonical Allele Identifier: CA276206

Gene:

Linked Data

• ClinVar Variation Id: 209230
• ClinVar RCV Id: RCV000191173
• dbSNP Id: rs8176323
• gnomAD v2: 17-41195711-G-C
• gnomAD v3: 17-43043694-G-C
• gnomAD v4: 17-43043694-G-C
• MyVariant Identifiers: chr17:g.41195711G>C (hg19) ; chr17:g.43043694G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43043694G>C , CM000679.2:g.43043694G>C	GRCh38
NC_000017.10:g.41195711G>C , CM000679.1:g.41195711G>C	GRCh37
NC_000017.9:g.38449237G>C	NCBI36
NG_005905.2:g.174290C>G , LRG_292:g.174290C>G