Canonical Allele Identifier: CA276207

Gene:

Linked Data

• ClinVar Variation Id: 209231
• ClinVar RCV Id: RCV000191174
• dbSNP Id: rs8176322
• gnomAD v2: 17-41195773-A-G
• gnomAD v3: 17-43043756-A-G
• gnomAD v4: 17-43043756-A-G
• MyVariant Identifiers: chr17:g.41195773A>G (hg19) ; chr17:g.43043756A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43043756A>G , CM000679.2:g.43043756A>G	GRCh38
NC_000017.10:g.41195773A>G , CM000679.1:g.41195773A>G	GRCh37
NC_000017.9:g.38449299A>G	NCBI36
NG_005905.2:g.174228T>C , LRG_292:g.174228T>C