Canonical Allele Identifier: CA13857988

Gene:

Linked Data

• ClinVar Variation Id: 1290099
• ClinVar RCV Id: RCV001714982
• dbSNP Id: rs9548868
• gnomAD v2: 13-40229585-C-T
• gnomAD v3: 13-39655448-C-T
• gnomAD v4: 13-39655448-C-T
• MyVariant Identifiers: chr13:g.40229585C>T (hg19) ; chr13:g.39655448C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.39655448C>T , CM000675.2:g.39655448C>T	GRCh38
NC_000013.10:g.40229585C>T , CM000675.1:g.40229585C>T	GRCh37
NC_000013.9:g.39127585C>T	NCBI36
NG_028352.1:g.4822C>T