Allele Registry

Canonical Allele Identifier: CA11162695

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr2:g.135787729A>G

GRCh37 chr2:g.136545299A>G

Linked Data - Sequence & Population

gnomAD v2:

2:136545299 A / G

gnomAD v3:

2:135787729 A / G

gnomAD v4:

chr2-135787729-A-G

Joint Max Group AF 0.11360738 (AFR)

Genomes Max Group AF 0.11363559 (AFR)

Exomes Max Group AF 0.01707859 (EAS)

Linked Data - NCBI & NCI

dbSNP:

16832011

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135787729A>G , CM000664.2:g.135787729A>G	GRCh38
NC_000002.11:g.136545299A>G , CM000664.1:g.136545299A>G	GRCh37
NC_000002.10:g.136261769A>G	NCBI36
NG_008104.2:g.72441T>C , LRG_338:g.72441T>C

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