Allele Registry

Canonical Allele Identifier: CA16590156

Gene:

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chr21:g.21992812T>C

GRCh37 chr21:g.23365131T>C

Linked Data - Sequence & Population

gnomAD v2:

21:23365131 T / C

gnomAD v3:

21:21992812 T / C

gnomAD v4:

chr21-21992812-T-C

Joint Max Group AF 0.58586674 (EAS)

Genomes Max Group AF 0.58586674 (EAS)

Linked Data - NCBI & NCI

dbSNP:

2827196

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.21992812T>C , CM000683.2:g.21992812T>C	GRCh38
NC_000021.8:g.23365131T>C , CM000683.1:g.23365131T>C	GRCh37
NC_000021.7:g.22287002T>C	NCBI36

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