ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA562330755
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.123439091G>T
GRCh37
chr5:g.122774785G>T
Linked Data - Sequence & Population
gnomAD v2:
5:122774785 G / T
gnomAD v3:
5:123439091 G / T
gnomAD v4:
chr5-123439091-G-T
Joint Max Group AF
0.00006837 (EAS)
Genomes Max Group AF
0.00006837 (EAS)
Linked Data - NCBI & NCI
dbSNP:
7705033
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.123439091G>T , CM000667.2:g.123439091G>T
GRCh38
NC_000005.9:g.122774785G>T , CM000667.1:g.122774785G>T
GRCh37
NC_000005.8:g.122802684G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'