ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA13002641
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.133635081C>T
GRCh37
chr9:g.136500203C>T
Linked Data - Sequence & Population
gnomAD v2:
9:136500203 C / T
gnomAD v3:
9:133635081 C / T
gnomAD v4:
chr9-133635081-C-T
Joint Max Group AF
0.64962719 (EAS)
Genomes Max Group AF
0.64962719 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1611114
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.133635081C>T , CM000671.2:g.133635081C>T
GRCh38
NC_000009.11:g.136500203C>T , CM000671.1:g.136500203C>T
GRCh37
NC_000009.10:g.135490024C>T
NCBI36
NG_008645.1:g.3719C>T
Search 100 bp 5'
Search 100 bp 3'