ClinGen Allele Registry
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Canonical Allele Identifier:
CA12017592
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.175448999G>A
GRCh37
chr5:g.174876002G>A
Linked Data - Sequence & Population
gnomAD v2:
5:174876002 G / A
gnomAD v3:
5:175448999 G / A
gnomAD v4:
chr5-175448999-G-A
Joint Max Group AF
0.37575499 (EAS)
Genomes Max Group AF
0.37575499 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2168631
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.175448999G>A , CM000667.2:g.175448999G>A
GRCh38
NC_000005.9:g.174876002G>A , CM000667.1:g.174876002G>A
GRCh37
NC_000005.8:g.174808608G>A
NCBI36
NG_011802.1:g.162C>T
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