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Canonical Allele Identifier:
CA13695638
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.108349043G>T
GRCh37
chr12:g.108742820G>T
Linked Data - Sequence & Population
gnomAD v2:
12:108742820 G / T
gnomAD v3:
12:108349043 G / T
gnomAD v4:
chr12-108349043-G-T
Joint Max Group AF
0.08527882 (AFR)
Genomes Max Group AF
0.08527882 (AFR)
Linked Data - NCBI & NCI
dbSNP:
17040430
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.108349043G>T , CM000674.2:g.108349043G>T
GRCh38
NC_000012.11:g.108742820G>T , CM000674.1:g.108742820G>T
GRCh37
NC_000012.10:g.107266950G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'