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Canonical Allele Identifier:
CA244112177
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.114266710G>T
GRCh37
chr12:g.114704515G>T
Linked Data - Sequence & Population
gnomAD v2:
12:114704515 G / T
gnomAD v3:
12:114266710 G / T
gnomAD v4:
chr12-114266710-G-T
Joint Max Group AF
0.00237406 (AMR)
Genomes Max Group AF
0.00237406 (AMR)
Linked Data - NCBI & NCI
ClinVar RCV:
RCV003934482
ClinVar Variation:
3046110
dbSNP:
141875471
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.114266710G>T , CM000674.2:g.114266710G>T
GRCh38
NC_000012.11:g.114704515G>T , CM000674.1:g.114704515G>T
GRCh37
NC_000012.10:g.113188898G>T
NCBI36
Search 100 bp 5'
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