ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA801838530
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.110854361G>T
GRCh37
chr5:g.110190060G>T
Linked Data - Sequence & Population
gnomAD v3:
5:110854361 G / T
gnomAD v4:
chr5-110854361-G-T
Joint Max Group AF
0.00001171 (NFE)
Genomes Max Group AF
0.00001171 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1271039603
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.110854361G>T , CM000667.2:g.110854361G>T
GRCh38
NC_000005.9:g.110190060G>T , CM000667.1:g.110190060G>T
GRCh37
NC_000005.8:g.110217959G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'