ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA95279776
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.34041798G>A
GRCh37
chr4:g.34043420G>A
Linked Data - Sequence & Population
gnomAD v2:
4:34043420 G / A
gnomAD v3:
4:34041798 G / A
gnomAD v4:
chr4-34041798-G-A
Joint Max Group AF
0.35835521 (AFR)
Genomes Max Group AF
0.35835521 (AFR)
Linked Data - NCBI & NCI
dbSNP:
13106616
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.34041798G>A , CM000666.2:g.34041798G>A
GRCh38
NC_000004.11:g.34043420G>A , CM000666.1:g.34043420G>A
GRCh37
NC_000004.10:g.33719815G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'