ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA12527176
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.155969463G>A
GRCh37
chr7:g.155762157G>A
Linked Data - Sequence & Population
gnomAD v2:
7:155762157 G / A
gnomAD v3:
7:155969463 G / A
gnomAD v4:
chr7-155969463-G-A
Joint Max Group AF
0.28294728 (EAS)
Genomes Max Group AF
0.28294728 (EAS)
Linked Data - NCBI & NCI
dbSNP:
6943029
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.155969463G>A , CM000669.2:g.155969463G>A
GRCh38
NC_000007.13:g.155762157G>A , CM000669.1:g.155762157G>A
GRCh37
NC_000007.12:g.155454918G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'