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Canonical Allele Identifier:
CA11701902
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr4:g.137832570T>C
GRCh37
chr4:g.138753724T>C
Linked Data - Sequence & Population
gnomAD v2:
4:138753724 T / C
gnomAD v3:
4:137832570 T / C
gnomAD v4:
chr4-137832570-T-C
Joint Max Group AF
0.92618065 (SAS)
Genomes Max Group AF
0.92618065 (SAS)
Linked Data - NCBI & NCI
dbSNP:
1509269
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.137832570T>C , CM000666.2:g.137832570T>C
GRCh38
NC_000004.11:g.138753724T>C , CM000666.1:g.138753724T>C
GRCh37
NC_000004.10:g.138973174T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'