Allele Registry

Canonical Allele Identifier: CA16100478

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr2:g.64800490T>C

GRCh37 chr2:g.65027624T>C

Linked Data - Sequence & Population

gnomAD v2:

2:65027624 T / C

gnomAD v3:

2:64800490 T / C

gnomAD v4:

chr2-64800490-T-C

Joint Max Group AF 0.392097 (SAS)

Genomes Max Group AF 0.392097 (SAS)

Linked Data - NCBI & NCI

dbSNP:

11683197

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.64800490T>C , CM000664.2:g.64800490T>C	GRCh38
NC_000002.11:g.65027624T>C , CM000664.1:g.65027624T>C	GRCh37
NC_000002.10:g.64881128T>C	NCBI36

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