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Canonical Allele Identifier:
CA13766777
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.84852893C>T
GRCh37
chr12:g.85246672C>T
Linked Data - Sequence & Population
gnomAD v2:
12:85246672 C / T
gnomAD v3:
12:84852893 C / T
gnomAD v4:
chr12-84852893-C-T
Joint Max Group AF
0.53029774 (AFR)
Genomes Max Group AF
0.53029774 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7968722
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.84852893C>T , CM000674.2:g.84852893C>T
GRCh38
NC_000012.11:g.85246672C>T , CM000674.1:g.85246672C>T
GRCh37
NC_000012.10:g.83770803C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'