Canonical Allele Identifier: CA219610035

Gene:

Linked Data

• dbSNP Id: rs1054395641
• gnomAD v2: 11-33806767-G-C
• gnomAD v3: 11-33785221-G-C
• gnomAD v4: 11-33785221-G-C
• MyVariant Identifiers: chr11:g.33806767G>C (hg19) ; chr11:g.33785221G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.33785221G>C , CM000673.2:g.33785221G>C	GRCh38
NC_000011.9:g.33806767G>C , CM000673.1:g.33806767G>C	GRCh37
NC_000011.8:g.33763343G>C	NCBI36