ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA195119359
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.81400122C>T
GRCh38
chr9:g.81400122_81400128delinsTATTTTT
GRCh37
chr9:g.84015037C>T
GRCh37
chr9:g.84015037_84015043delinsTATTTTT
Linked Data - Sequence & Population
gnomAD v2:
9:84015037 C / T
gnomAD v3:
9:81400122 C / T
gnomAD v4:
chr9-81400122-C-T
Joint Max Group AF
0.16840087 (NFE)
Genomes Max Group AF
0.16840087 (NFE)
Linked Data - NCBI & NCI
dbSNP:
10867752
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.81400122C>T , CM000671.2:g.81400122C>T
GRCh38
NC_000009.11:g.84015037C>T , CM000671.1:g.84015037C>T
GRCh37
NC_000009.10:g.83204857C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'