ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA129850834
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.159387493T>G
GRCh37
chr5:g.158814501T>G
Linked Data - Sequence & Population
gnomAD v2:
5:158814501 T / G
gnomAD v3:
5:159387493 T / G
gnomAD v4:
chr5-159387493-T-G
Joint Max Group AF
0.000008 (AFR)
Genomes Max Group AF
0.000008 (AFR)
Linked Data - NCBI & NCI
dbSNP:
915965089
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.159387493T>G , CM000667.2:g.159387493T>G
GRCh38
NC_000005.9:g.158814501T>G , CM000667.1:g.158814501T>G
GRCh37
NC_000005.8:g.158747079T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'