ClinGen Allele Registry
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Canonical Allele Identifier:
CA12113554
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.23243916C>T
GRCh37
chr5:g.23244025C>T
Linked Data - Sequence & Population
gnomAD v2:
5:23244025 C / T
gnomAD v3:
5:23243916 C / T
gnomAD v4:
chr5-23243916-C-T
Joint Max Group AF
0.34778284 (NFE)
Genomes Max Group AF
0.34778284 (NFE)
Linked Data - NCBI & NCI
dbSNP:
17376026
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.23243916C>T , CM000667.2:g.23243916C>T
GRCh38
NC_000005.9:g.23244025C>T , CM000667.1:g.23244025C>T
GRCh37
NC_000005.8:g.23279782C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'