Allele Registry

Canonical Allele Identifier: CA16229545

Gene:

Linked Data

ClinVar RCV:

RCV001661025

ClinVar Variation:

1252728

dbSNP:

10042486

gnomAD v2:

5:63261329 C / T

gnomAD v3:

5:63965502 C / T

gnomAD v4:

chr5-63965502-C-T

Joint Max Group AF 0.77214347 (EAS)

Genomes Max Group AF 0.77214347 (EAS)

MyVariant.info:

GRCh38 chr5:g.63965502C>T

GRCh37 chr5:g.63261329C>T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.63965502C>T , CM000667.2:g.63965502C>T	GRCh38
NC_000005.9:g.63261329C>T , CM000667.1:g.63261329C>T	GRCh37
NC_000005.8:g.63297085C>T	NCBI36
NG_032816.1:g.1791G>A

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