ClinGen Allele Registry
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Canonical Allele Identifier:
CA107087660
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.137405718G>A
GRCh37
chr4:g.138326872G>A
Linked Data - Sequence & Population
gnomAD v2:
4:138326872 G / A
gnomAD v3:
4:137405718 G / A
gnomAD v4:
chr4-137405718-G-A
Joint Max Group AF
0.6746075 (AFR)
Genomes Max Group AF
0.6746075 (AFR)
Linked Data - NCBI & NCI
dbSNP:
4416533
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.137405718G>A , CM000666.2:g.137405718G>A
GRCh38
NC_000004.11:g.138326872G>A , CM000666.1:g.138326872G>A
GRCh37
NC_000004.10:g.138546322G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'