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Canonical Allele Identifier:
CA13667456
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.51857488G>T
GRCh37
chr12:g.52251272G>T
Linked Data - Sequence & Population
gnomAD v2:
12:52251272 G / T
gnomAD v3:
12:51857488 G / T
gnomAD v4:
chr12-51857488-G-T
Joint Max Group AF
0.669018 (EAS)
Genomes Max Group AF
0.669018 (EAS)
Linked Data - NCBI & NCI
dbSNP:
7976059
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.51857488G>T , CM000674.2:g.51857488G>T
GRCh38
NC_000012.11:g.52251272G>T , CM000674.1:g.52251272G>T
GRCh37
NC_000012.10:g.50537539G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'