Allele Registry

Canonical Allele Identifier: CA10713956

Gene:

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chr1:g.8035440T>G

GRCh37 chr1:g.8095500T>G

Linked Data - Sequence & Population

gnomAD v2:

1:8095500 T / G

gnomAD v3:

1:8035440 T / G

gnomAD v4:

chr1-8035440-T-G

Joint Max Group AF 0.61257215 (EAS)

Genomes Max Group AF 0.61257215 (EAS)

Linked Data - NCBI & NCI

dbSNP:

225132

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8035440T>G , CM000663.2:g.8035440T>G	GRCh38
NC_000001.10:g.8095500T>G , CM000663.1:g.8095500T>G	GRCh37
NC_000001.9:g.8018087T>G	NCBI36

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