ClinGen Allele Registry
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Canonical Allele Identifier:
CA526915338
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.163063860C>T
GRCh37
chr1:g.163033650C>T
Linked Data - Sequence & Population
gnomAD v2:
1:163033650 C / T
gnomAD v3:
1:163063860 C / T
gnomAD v4:
chr1-163063860-C-T
Joint Max Group AF
0.00000488 (NFE)
Genomes Max Group AF
0.00000488 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1368293607
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.163063860C>T , CM000663.2:g.163063860C>T
GRCh38
NC_000001.10:g.163033650C>T , CM000663.1:g.163033650C>T
GRCh37
NC_000001.9:g.161300274C>T
NCBI36
NG_023312.1:g.255C>T
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