ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA116120662
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.26389153G>C
GRCh37
chr5:g.26389262G>C
Linked Data - Sequence & Population
gnomAD v2:
5:26389262 G / C
gnomAD v3:
5:26389153 G / C
gnomAD v4:
chr5-26389153-G-C
Joint Max Group AF
0.24708849 (EAS)
Genomes Max Group AF
0.24708849 (EAS)
Linked Data - NCBI & NCI
dbSNP:
969088
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.26389153G>C , CM000667.2:g.26389153G>C
GRCh38
NC_000005.9:g.26389262G>C , CM000667.1:g.26389262G>C
GRCh37
NC_000005.8:g.26425019G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'