Allele Registry

Canonical Allele Identifier: CA105233264

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr4:g.122589929C>T

GRCh37 chr4:g.123511084C>T

Linked Data - Sequence & Population

gnomAD v2:

4:123511084 C / T

gnomAD v3:

4:122589929 C / T

gnomAD v4:

chr4-122589929-C-T

Joint Max Group AF 0.000008 (AFR)

Genomes Max Group AF 0.000008 (AFR)

Linked Data - NCBI & NCI

dbSNP:

1051553649

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122589929C>T , CM000666.2:g.122589929C>T	GRCh38
NC_000004.11:g.123511084C>T , CM000666.1:g.123511084C>T	GRCh37
NC_000004.10:g.123730534C>T	NCBI36

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