ClinGen Allele Registry
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Canonical Allele Identifier:
CA683731160
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.112936701G>C
GRCh37
chr12:g.113374506G>C
Linked Data - Sequence & Population
gnomAD v3:
12:112936701 G / C
gnomAD v4:
chr12-112936701-G-C
Linked Data - NCBI & NCI
dbSNP:
12302655
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.112936701G>C , CM000674.2:g.112936701G>C
GRCh38
NC_000012.11:g.113374506G>C , CM000674.1:g.113374506G>C
GRCh37
NC_000012.10:g.111858889G>C
NCBI36
Search 100 bp 5'
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