Allele Registry

Canonical Allele Identifier: CA476867264

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr11:g.116813312T>A

GRCh37 chr11:g.116684028T>A

Linked Data - Sequence & Population

gnomAD v3:

11:116813312 T / A

gnomAD v4:

chr11-116813312-T-A

Linked Data - NCBI & NCI

dbSNP:

7396835

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116813312T>A , CM000673.2:g.116813312T>A	GRCh38
NC_000011.9:g.116684028T>A , CM000673.1:g.116684028T>A	GRCh37
NC_000011.8:g.116189238T>A	NCBI36

Search 100 bp 5'

Search 100 bp 3'