Canonical Allele Identifier: CA217112021

Gene:

Linked Data

• ClinVar Variation Id: 702013
• ClinVar RCV Id: RCV001001383 ; RCV000870817 ; RCV001078285
• dbSNP Id: rs113969885
• gnomAD v2: 11-5246646-C-T
• gnomAD v3: 11-5225416-C-T
• gnomAD v4: 11-5225416-C-T
• MyVariant Identifiers: chr11:g.5246646C>T (hg19) ; chr11:g.5225416C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5225416C>T , CM000673.2:g.5225416C>T	GRCh38
NC_000011.9:g.5246646C>T , CM000673.1:g.5246646C>T	GRCh37
NC_000011.8:g.5203222C>T	NCBI36
NG_000007.3:g.72200G>A
NG_059281.1:g.6656G>A