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Canonical Allele Identifier:
CA79152314
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.88475025C>T
GRCh37
chr3:g.88524175C>T
Linked Data - Sequence & Population
gnomAD v2:
3:88524175 C / T
gnomAD v3:
3:88475025 C / T
gnomAD v4:
chr3-88475025-C-T
Joint Max Group AF
0.46369066 (EAS)
Genomes Max Group AF
0.46369066 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2880961
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.88475025C>T , CM000665.2:g.88475025C>T
GRCh38
NC_000003.11:g.88524175C>T , CM000665.1:g.88524175C>T
GRCh37
NC_000003.10:g.88606865C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'