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Canonical Allele Identifier:
CA11427849
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.171039196T>G
GRCh37
chr3:g.170756985T>G
Linked Data - Sequence & Population
gnomAD v2:
3:170756985 T / G
gnomAD v3:
3:171039196 T / G
gnomAD v4:
chr3-171039196-T-G
Joint Max Group AF
0.46273525 (AFR)
Genomes Max Group AF
0.46273525 (AFR)
Linked Data - NCBI & NCI
dbSNP:
6785233
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.171039196T>G , CM000665.2:g.171039196T>G
GRCh38
NC_000003.11:g.170756985T>G , CM000665.1:g.170756985T>G
GRCh37
NC_000003.10:g.172239679T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'