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Canonical Allele Identifier:
CA11666049
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr4:g.161252328C>T
GRCh37
chr4:g.162173480C>T
Linked Data - Sequence & Population
gnomAD v2:
4:162173480 C / T
gnomAD v3:
4:161252328 C / T
gnomAD v4:
chr4-161252328-C-T
Joint Max Group AF
0.27123125 (EAS)
Genomes Max Group AF
0.27123125 (EAS)
Linked Data - NCBI & NCI
dbSNP:
7676384
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.161252328C>T , CM000666.2:g.161252328C>T
GRCh38
NC_000004.11:g.162173480C>T , CM000666.1:g.162173480C>T
GRCh37
NC_000004.10:g.162392930C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'