Canonical Allele Identifier: CA602182454

Gene:

Linked Data

• ClinVar Variation Id: 1437315
• ClinVar RCV Id: RCV001948697
• dbSNP Id: rs1417977595
• gnomAD v2: 11-118955413-C-T
• gnomAD v3: 11-119084703-C-T
• gnomAD v4: 11-119084703-C-T
• MyVariant Identifiers: chr11:g.118955413C>T (hg19) ; chr11:g.119084703C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119084703C>T , CM000673.2:g.119084703C>T	GRCh38
NC_000011.9:g.118955413C>T , CM000673.1:g.118955413C>T	GRCh37
NC_000011.8:g.118460623C>T	NCBI36
NG_008093.1:g.4827C>T