ClinGen Allele Registry
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Canonical Allele Identifier:
CA683206356
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.106987362C>T
GRCh37
chr12:g.107381140C>T
Linked Data - Sequence & Population
gnomAD v3:
12:106987362 C / T
gnomAD v4:
chr12-106987362-C-T
Linked Data - NCBI & NCI
dbSNP:
2287161
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.106987362C>T , CM000674.2:g.106987362C>T
GRCh38
NC_000012.11:g.107381140C>T , CM000674.1:g.107381140C>T
GRCh37
NC_000012.10:g.105905270C>T
NCBI36
Search 100 bp 5'
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