ClinGen Allele Registry
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Canonical Allele Identifier:
CA157514646
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.37580319T>C
GRCh37
chr7:g.37619922T>C
Linked Data - Sequence & Population
gnomAD v2:
7:37619922 T / C
gnomAD v3:
7:37580319 T / C
gnomAD v4:
chr7-37580319-T-C
Joint Max Group AF
0.73469128 (EAS)
Genomes Max Group AF
0.73469128 (EAS)
Linked Data - NCBI & NCI
dbSNP:
17265593
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.37580319T>C , CM000669.2:g.37580319T>C
GRCh38
NC_000007.13:g.37619922T>C , CM000669.1:g.37619922T>C
GRCh37
NC_000007.12:g.37586447T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'