Allele Registry

Canonical Allele Identifier: CA14910638

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr21:g.39835868G>A

GRCh37 chr21:g.41207795G>A

Linked Data - Sequence & Population

gnomAD v2:

21:41207795 G / A

gnomAD v3:

21:39835868 G / A

gnomAD v4:

chr21-39835868-G-A

Joint Max Group AF 0.30513095 (AFR)

Genomes Max Group AF 0.30513095 (AFR)

Linked Data - NCBI & NCI

dbSNP:

741864

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.39835868G>A , CM000683.2:g.39835868G>A	GRCh38
NC_000021.8:g.41207795G>A , CM000683.1:g.41207795G>A	GRCh37
NC_000021.7:g.40129665G>A	NCBI36

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