Canonical Allele Identifier: CA13386904

Gene:

Linked Data

• ClinVar Variation Id: 1294696
• ClinVar RCV Id: RCV001720600
• dbSNP Id: rs10898853
• gnomAD v2: 11-70049253-T-C
• gnomAD v3: 11-70203147-T-C
• gnomAD v4: 11-70203147-T-C
• MyVariant Identifiers: chr11:g.70049253T>C (hg19) ; chr11:g.70203147T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70203147T>C , CM000673.2:g.70203147T>C	GRCh38
NC_000011.9:g.70049253T>C , CM000673.1:g.70049253T>C	GRCh37
NC_000011.8:g.69726901T>C	NCBI36
NG_027966.1:g.4985T>C , LRG_228:g.4985T>C