ClinGen Allele Registry
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Canonical Allele Identifier:
CA11989659
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.173237160G>A
GRCh37
chr5:g.172664163G>A
Linked Data - Sequence & Population
gnomAD v2:
5:172664163 G / A
gnomAD v3:
5:173237160 G / A
gnomAD v4:
chr5-173237160-G-A
Joint Max Group AF
0.61865056 (EAS)
Genomes Max Group AF
0.61865056 (EAS)
Linked Data - NCBI & NCI
dbSNP:
6882776
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.173237160G>A , CM000667.2:g.173237160G>A
GRCh38
NC_000005.9:g.172664163G>A , CM000667.1:g.172664163G>A
GRCh37
NC_000005.8:g.172596769G>A
NCBI36
NG_013340.1:g.3153C>T
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