Canonical Allele Identifier: CA10587123

Gene:

Linked Data

• ClinVar Variation Id: 256343
• ClinVar RCV Id: RCV000252325
• dbSNP Id: rs112988270
• gnomAD v2: 11-5246475-C-T
• gnomAD v3: 11-5225245-C-T
• gnomAD v4: 11-5225245-C-T
• MyVariant Identifiers: chr11:g.5246475C>T (hg19) ; chr11:g.5225245C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5225245C>T , CM000673.2:g.5225245C>T	GRCh38
NC_000011.9:g.5246475C>T , CM000673.1:g.5246475C>T	GRCh37
NC_000011.8:g.5203051C>T	NCBI36
NG_000007.3:g.72371G>A
NG_059281.1:g.6827G>A