ClinGen Allele Registry
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Canonical Allele Identifier:
CA31810358
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.163063853G>A
GRCh37
chr1:g.163033643G>A
Linked Data - Sequence & Population
gnomAD v2:
1:163033643 G / A
gnomAD v3:
1:163063853 G / A
gnomAD v4:
chr1-163063853-G-A
Linked Data - NCBI & NCI
dbSNP:
1018301889
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.163063853G>A , CM000663.2:g.163063853G>A
GRCh38
NC_000001.10:g.163033643G>A , CM000663.1:g.163033643G>A
GRCh37
NC_000001.9:g.161300267G>A
NCBI36
NG_023312.1:g.248G>A
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