Allele Registry

Canonical Allele Identifier: CA11677035

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr4:g.4865595T>G

GRCh37 chr4:g.4867322T>G

Linked Data - Sequence & Population

gnomAD v2:

4:4867322 T / G

gnomAD v3:

4:4865595 T / G

gnomAD v4:

chr4-4865595-T-G

Joint Max Group AF 0.72185798 (AFR)

Genomes Max Group AF 0.72185798 (AFR)

Linked Data - NCBI & NCI

dbSNP:

4464513

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.4865595T>G , CM000666.2:g.4865595T>G	GRCh38
NC_000004.11:g.4867322T>G , CM000666.1:g.4867322T>G	GRCh37
NC_000004.10:g.4918223T>G	NCBI36
NG_008121.1:g.10931T>G

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