Canonical Allele Identifier: CA12857375

Gene:

Linked Data

• ClinVar Variation Id: 1179394
• ClinVar RCV Id: RCV001536371
• dbSNP Id: rs73663168
• gnomAD v2: 8-11422180-C-T
• gnomAD v3: 8-11564671-C-T
• gnomAD v4: 8-11564671-C-T
• MyVariant Identifiers: chr8:g.11422180C>T (hg19) ; chr8:g.11564671C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564671C>T , CM000670.2:g.11564671C>T	GRCh38
NC_000008.10:g.11422180C>T , CM000670.1:g.11422180C>T	GRCh37
NC_000008.9:g.11459589C>T	NCBI36
NG_023543.1:g.75660C>T
NG_023543.2:g.75660C>T