ClinGen Allele Registry
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Canonical Allele Identifier:
CA11292058
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr2:g.203874215G>A
GRCh37
chr2:g.204738938G>A
Linked Data - Sequence & Population
gnomAD v2:
2:204738938 G / A
gnomAD v3:
2:203874215 G / A
gnomAD v4:
chr2-203874215-G-A
Joint Max Group AF
0.1726329 (AFR)
Genomes Max Group AF
0.1726329 (AFR)
Linked Data - NCBI & NCI
dbSNP:
11571319
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.203874215G>A , CM000664.2:g.203874215G>A
GRCh38
NC_000002.11:g.204738938G>A , CM000664.1:g.204738938G>A
GRCh37
NC_000002.10:g.204447183G>A
NCBI36
NG_011502.1:g.11430G>A
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