Canonical Allele Identifier: CA276195

Gene:

Linked Data

• ClinVar Variation Id: 209219
• ClinVar RCV Id: RCV000191162
• dbSNP Id: rs78603756
• gnomAD v2: 17-41191488-G-A
• gnomAD v3: 17-43039471-G-A
• gnomAD v4: 17-43039471-G-A
• MyVariant Identifiers: chr17:g.41191488G>A (hg19) ; chr17:g.43039471G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43039471G>A , CM000679.2:g.43039471G>A	GRCh38
NC_000017.10:g.41191488G>A , CM000679.1:g.41191488G>A	GRCh37
NC_000017.9:g.38445014G>A	NCBI36
NG_005905.2:g.178513C>T , LRG_292:g.178513C>T