ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA10963804
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.169630994T>C
GRCh37
chr1:g.169600232T>C
Linked Data - Sequence & Population
gnomAD v2:
1:169600232 T / C
gnomAD v3:
1:169630994 T / C
gnomAD v4:
chr1-169630994-T-C
Joint Max Group AF
0.51393485 (AFR)
Genomes Max Group AF
0.51393485 (AFR)
Linked Data - NCBI & NCI
dbSNP:
3753306
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.169630994T>C , CM000663.2:g.169630994T>C
GRCh38
NC_000001.10:g.169600232T>C , CM000663.1:g.169600232T>C
GRCh37
NC_000001.9:g.167866856T>C
NCBI36
NG_012125.1:g.4146A>G
NG_012125.2:g.4146A>G
Search 100 bp 5'
Search 100 bp 3'