Allele Registry

Canonical Allele Identifier: CA168954461

Gene:

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chr7:g.149506571A>C

GRCh37 chr7:g.149203662A>C

Linked Data - Sequence & Population

gnomAD v2:

7:149203662 A / C

gnomAD v3:

7:149506571 A / C

gnomAD v4:

chr7-149506571-A-C

Joint Max Group AF 0.981854 (AFR)

Genomes Max Group AF 0.981854 (AFR)

Linked Data - NCBI & NCI

dbSNP:

855913

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.149506571A>C , CM000669.2:g.149506571A>C	GRCh38
NC_000007.13:g.149203662A>C , CM000669.1:g.149203662A>C	GRCh37
NC_000007.12:g.148834595A>C	NCBI36

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