Canonical Allele Identifier: CA32418407

Gene:

Linked Data

• ClinVar Variation Id: 1279267
• ClinVar RCV Id: RCV001690988
• dbSNP Id: rs16862404
• gnomAD v2: 1-169555973-G-C
• gnomAD v3: 1-169586735-G-C
• gnomAD v4: 1-169586735-G-C
• MyVariant Identifiers: chr1:g.169555973G>C (hg19) ; chr1:g.169586735G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169586735G>C , CM000663.2:g.169586735G>C	GRCh38
NC_000001.10:g.169555973G>C , CM000663.1:g.169555973G>C	GRCh37
NC_000001.9:g.167822597G>C	NCBI36
NG_011806.1:g.4797C>G , LRG_553:g.4797C>G