ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA25990423
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.80445429G>A
GRCh37
chr1:g.80911114G>A
Linked Data - Sequence & Population
gnomAD v2:
1:80911114 G / A
gnomAD v3:
1:80445429 G / A
gnomAD v4:
chr1-80445429-G-A
Joint Max Group AF
0.13907003 (AFR)
Genomes Max Group AF
0.13907003 (AFR)
Linked Data - NCBI & NCI
dbSNP:
12118390
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.80445429G>A , CM000663.2:g.80445429G>A
GRCh38
NC_000001.10:g.80911114G>A , CM000663.1:g.80911114G>A
GRCh37
NC_000001.9:g.80683702G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'