ClinGen Allele Registry
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Canonical Allele Identifier:
CA890355469
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.163063858C>G
GRCh37
chr1:g.163033648C>G
Linked Data - Sequence & Population
gnomAD v3:
1:163063858 C / G
gnomAD v4:
chr1-163063858-C-G
Linked Data - NCBI & NCI
dbSNP:
1227970606
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.163063858C>G , CM000663.2:g.163063858C>G
GRCh38
NC_000001.10:g.163033648C>G , CM000663.1:g.163033648C>G
GRCh37
NC_000001.9:g.161300272C>G
NCBI36
NG_023312.1:g.253C>G
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