Canonical Allele Identifier: CA32667089

Gene:

Linked Data

• ClinVar Variation Id: 1260300
• ClinVar RCV Id: RCV001659578
• dbSNP Id: rs2075648
• gnomAD v2: 1-171621834-C-T
• gnomAD v3: 1-171652694-C-T
• gnomAD v4: 1-171652694-C-T
• MyVariant Identifiers: chr1:g.171621834C>T (hg19) ; chr1:g.171652694C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171652694C>T , CM000663.2:g.171652694C>T	GRCh38
NC_000001.10:g.171621834C>T , CM000663.1:g.171621834C>T	GRCh37
NC_000001.9:g.169888457C>T	NCBI36
NG_008859.1:g.4940G>A