ClinGen Allele Registry
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Canonical Allele Identifier:
CA537451952
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.164038051T>A
GRCh37
chr2:g.164894561T>A
Linked Data - Sequence & Population
gnomAD v2:
2:164894561 T / A
Linked Data - NCBI & NCI
dbSNP:
12692709
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.164038051T>A , CM000664.2:g.164038051T>A
GRCh38
NC_000002.11:g.164894561T>A , CM000664.1:g.164894561T>A
GRCh37
NC_000002.10:g.164602807T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'