ClinGen Allele Registry
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Canonical Allele Identifier:
CA531013793
Gene:
Linked Data - Expert Curation
COSMIC:
COSN22460822
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.11897401A>T
GRCh37
chr2:g.12037527A>T
Linked Data - Sequence & Population
gnomAD v2:
2:12037527 A / T
gnomAD v3:
2:11897401 A / T
gnomAD v4:
chr2-11897401-A-T
Linked Data - NCBI & NCI
dbSNP:
1318520713
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.11897401A>T , CM000664.2:g.11897401A>T
GRCh38
NC_000002.11:g.12037527A>T , CM000664.1:g.12037527A>T
GRCh37
NC_000002.10:g.11954978A>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'