ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA201360896
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.3797822G>T
GRCh37
chr10:g.3840014G>T
Linked Data - Sequence & Population
gnomAD v2:
10:3840014 G / T
gnomAD v3:
10:3797822 G / T
gnomAD v4:
chr10-3797822-G-T
Joint Max Group AF
0.29237519 (SAS)
Genomes Max Group AF
0.29237519 (SAS)
Linked Data - NCBI & NCI
dbSNP:
10508266
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.3797822G>T , CM000672.2:g.3797822G>T
GRCh38
NC_000010.10:g.3840014G>T , CM000672.1:g.3840014G>T
GRCh37
NC_000010.9:g.3830014G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'