Canonical Allele Identifier: CA13369111

Gene:

Linked Data

• dbSNP Id: rs747302
• gnomAD v2: 11-636689-G-C
• gnomAD v3: 11-636689-G-C
• gnomAD v4: 11-636689-G-C
• MyVariant Identifiers: chr11:g.636689G>C (hg19) ; chr11:g.636689G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.636689G>C , CM000673.2:g.636689G>C	GRCh38
NC_000011.9:g.636689G>C , CM000673.1:g.636689G>C	GRCh37
NC_000011.8:g.626689G>C	NCBI36
NG_021241.1:g.4385G>C