ClinGen Allele Registry
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Canonical Allele Identifier:
CA12105495
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.123439091G>C
GRCh37
chr5:g.122774785G>C
Linked Data - Sequence & Population
gnomAD v2:
5:122774785 G / C
gnomAD v3:
5:123439091 G / C
gnomAD v4:
chr5-123439091-G-C
Joint Max Group AF
0.39082537 (AFR)
Genomes Max Group AF
0.39082537 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7705033
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.123439091G>C , CM000667.2:g.123439091G>C
GRCh38
NC_000005.9:g.122774785G>C , CM000667.1:g.122774785G>C
GRCh37
NC_000005.8:g.122802684G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'