ClinGen Allele Registry
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Canonical Allele Identifier:
CA12138767
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr5:g.175591132G>A
GRCh37
chr5:g.175018135G>A
Linked Data - Sequence & Population
gnomAD v2:
5:175018135 G / A
gnomAD v3:
5:175591132 G / A
gnomAD v4:
chr5-175591132-G-A
Joint Max Group AF
0.7862209 (SAS)
Genomes Max Group AF
0.7862209 (SAS)
Linked Data - NCBI & NCI
dbSNP:
1472606
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.175591132G>A , CM000667.2:g.175591132G>A
GRCh38
NC_000005.9:g.175018135G>A , CM000667.1:g.175018135G>A
GRCh37
NC_000005.8:g.174950741G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'