Canonical Allele Identifier: CA276196

Gene:

Linked Data

• ClinVar Variation Id: 209220
• ClinVar RCV Id: RCV000191163
• dbSNP Id: rs150356989
• gnomAD v2: 17-41191835-G-A
• gnomAD v3: 17-43039818-G-A
• gnomAD v4: 17-43039818-G-A
• MyVariant Identifiers: chr17:g.41191835G>A (hg19) ; chr17:g.43039818G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43039818G>A , CM000679.2:g.43039818G>A	GRCh38
NC_000017.10:g.41191835G>A , CM000679.1:g.41191835G>A	GRCh37
NC_000017.9:g.38445361G>A	NCBI36
NG_005905.2:g.178166C>T , LRG_292:g.178166C>T