ClinGen Allele Registry
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Canonical Allele Identifier:
CA901746450
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.162351221G>C
GRCh37
chr3:g.162069009G>C
Linked Data - NCBI & NCI
dbSNP:
12493123
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.162351221G>C , CM000665.2:g.162351221G>C
GRCh38
NC_000003.11:g.162069009G>C , CM000665.1:g.162069009G>C
GRCh37
NC_000003.10:g.163551703G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'