ClinGen Allele Registry
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Canonical Allele Identifier:
CA11949968
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.159395637G>C
GRCh37
chr5:g.158822645G>C
Linked Data - Sequence & Population
gnomAD v2:
5:158822645 G / C
gnomAD v3:
5:159395637 G / C
gnomAD v4:
chr5-159395637-G-C
Joint Max Group AF
0.41296927 (EAS)
Genomes Max Group AF
0.41296927 (EAS)
Linked Data - NCBI & NCI
dbSNP:
6887695
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.159395637G>C , CM000667.2:g.159395637G>C
GRCh38
NC_000005.9:g.158822645G>C , CM000667.1:g.158822645G>C
GRCh37
NC_000005.8:g.158755223G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'