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Canonical Allele Identifier:
CA105257182
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr4:g.122817391C>T
GRCh37
chr4:g.123738546C>T
Linked Data - Sequence & Population
gnomAD v2:
4:123738546 C / T
gnomAD v3:
4:122817391 C / T
gnomAD v4:
chr4-122817391-C-T
Joint Max Group AF
0.75557018 (AFR)
Genomes Max Group AF
0.75557018 (AFR)
Linked Data - NCBI & NCI
dbSNP:
308447
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.122817391C>T , CM000666.2:g.122817391C>T
GRCh38
NC_000004.11:g.123738546C>T , CM000666.1:g.123738546C>T
GRCh37
NC_000004.10:g.123957996C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'