ClinGen Allele Registry
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Canonical Allele Identifier:
CA169348153
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.155178759G>C
GRCh37
chr7:g.154970469G>C
Linked Data - Sequence & Population
gnomAD v2:
7:154970469 G / C
gnomAD v3:
7:155178759 G / C
gnomAD v4:
chr7-155178759-G-C
Joint Max Group AF
0.91264373 (NFE)
Genomes Max Group AF
0.91264373 (NFE)
Linked Data - NCBI & NCI
dbSNP:
10263087
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.155178759G>C , CM000669.2:g.155178759G>C
GRCh38
NC_000007.13:g.154970469G>C , CM000669.1:g.154970469G>C
GRCh37
NC_000007.12:g.154601402G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'