Allele Registry

Canonical Allele Identifier: CA249798

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr6:g.135105435A>G

GRCh37 chr6:g.135426573A>G

Linked Data - Sequence & Population

gnomAD v2:

6:135426573 A / G

gnomAD v3:

6:135105435 A / G

gnomAD v4:

chr6-135105435-A-G

Joint Max Group AF 0.26880104 (EAS)

Genomes Max Group AF 0.26880104 (EAS)

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000119308

ClinVar Variation:

132871

dbSNP:

4895441

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.135105435A>G , CM000668.2:g.135105435A>G	GRCh38
NC_000006.11:g.135426573A>G , CM000668.1:g.135426573A>G	GRCh37
NC_000006.10:g.135468266A>G	NCBI36

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