ClinGen Allele Registry
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Canonical Allele Identifier:
CA11297605
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.203874196G>A
GRCh37
chr2:g.204738919G>A
Linked Data - Sequence & Population
gnomAD v2:
2:204738919 G / A
gnomAD v3:
2:203874196 G / A
gnomAD v4:
chr2-203874196-G-A
Joint Max Group AF
0.5878951 (SAS)
Genomes Max Group AF
0.5878951 (SAS)
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000018429
RCV000018430
RCV001254798
RCV001515646
ClinVar Variation:
16922
dbSNP:
3087243
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.203874196G>A , CM000664.2:g.203874196G>A
GRCh38
NC_000002.11:g.204738919G>A , CM000664.1:g.204738919G>A
GRCh37
NC_000002.10:g.204447164G>A
NCBI36
NG_011502.1:g.11411G>A
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