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Canonical Allele Identifier:
CA13686473
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.42767023C>T
GRCh37
chr12:g.43160825C>T
Linked Data - Sequence & Population
gnomAD v2:
12:43160825 C / T
gnomAD v3:
12:42767023 C / T
gnomAD v4:
chr12-42767023-C-T
Joint Max Group AF
0.32440585 (EAS)
Genomes Max Group AF
0.32440585 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2731006
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.42767023C>T , CM000674.2:g.42767023C>T
GRCh38
NC_000012.11:g.43160825C>T , CM000674.1:g.43160825C>T
GRCh37
NC_000012.10:g.41447092C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'