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Canonical Allele Identifier:
CA16242177
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.130607626T>C
GRCh37
chr5:g.129943319T>C
Linked Data - Sequence & Population
gnomAD v2:
5:129943319 T / C
gnomAD v3:
5:130607626 T / C
gnomAD v4:
chr5-130607626-T-C
Joint Max Group AF
0.38589995 (EAS)
Genomes Max Group AF
0.38589995 (EAS)
Linked Data - NCBI & NCI
dbSNP:
7731657
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.130607626T>C , CM000667.2:g.130607626T>C
GRCh38
NC_000005.9:g.129943319T>C , CM000667.1:g.129943319T>C
GRCh37
NC_000005.8:g.129971218T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'