ClinGen Allele Registry
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Canonical Allele Identifier:
CA87508607
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.168007561A>G
GRCh37
chr3:g.167725349A>G
Linked Data - Sequence & Population
gnomAD v2:
3:167725349 A / G
gnomAD v3:
3:168007561 A / G
gnomAD v4:
chr3-168007561-A-G
Joint Max Group AF
0.42771299 (AFR)
Genomes Max Group AF
0.42771299 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7632500
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.168007561A>G , CM000665.2:g.168007561A>G
GRCh38
NC_000003.11:g.167725349A>G , CM000665.1:g.167725349A>G
GRCh37
NC_000003.10:g.169208043A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_001741013.1:n.1515A>G
Search 100 bp 5'
Search 100 bp 3'