ClinGen Allele Registry
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Canonical Allele Identifier:
CA755818525
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.11897366G>C
GRCh37
chr2:g.12037492G>C
Linked Data - NCBI & NCI
dbSNP:
4027132
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.11897366G>C , CM000664.2:g.11897366G>C
GRCh38
NC_000002.11:g.12037492G>C , CM000664.1:g.12037492G>C
GRCh37
NC_000002.10:g.11954943G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'