Canonical Allele Identifier: CA13443702

Gene:

Linked Data

• ClinVar Variation Id: 1249154
• ClinVar RCV Id: RCV001656675
• dbSNP Id: rs36211088
• gnomAD v2: 11-67350999-C-A
• gnomAD v3: 11-67583528-C-A
• gnomAD v4: 11-67583528-C-A
• MyVariant Identifiers: chr11:g.67350999C>A (hg19) ; chr11:g.67583528C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67583528C>A , CM000673.2:g.67583528C>A	GRCh38
NC_000011.9:g.67350999C>A , CM000673.1:g.67350999C>A	GRCh37
NC_000011.8:g.67107575C>A	NCBI36
NG_012075.1:g.4934C>A , LRG_723:g.4934C>A