ClinGen Allele Registry
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Canonical Allele Identifier:
CA31810394
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.163063897C>T
GRCh37
chr1:g.163033687C>T
Linked Data - Sequence & Population
gnomAD v3:
1:163063897 C / T
gnomAD v4:
chr1-163063897-C-T
Joint Max Group AF
0.00005293 (AMR)
Genomes Max Group AF
0.00005293 (AMR)
Linked Data - NCBI & NCI
dbSNP:
907767503
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.163063897C>T , CM000663.2:g.163063897C>T
GRCh38
NC_000001.10:g.163033687C>T , CM000663.1:g.163033687C>T
GRCh37
NC_000001.9:g.161300311C>T
NCBI36
NG_023312.1:g.292C>T
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