ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA198901289
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.114806799G>T
GRCh37
chr9:g.117569079G>T
Linked Data - Sequence & Population
gnomAD v3:
9:114806799 G / T
gnomAD v4:
chr9-114806799-G-T
Joint Max Group AF
0.00001921 (AFR)
Genomes Max Group AF
0.00001921 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1031433074
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.114806799G>T , CM000671.2:g.114806799G>T
GRCh38
NC_000009.11:g.117569079G>T , CM000671.1:g.117569079G>T
GRCh37
NC_000009.10:g.116608900G>T
NCBI36
NG_011488.2:g.4330C>A
Search 100 bp 5'
Search 100 bp 3'