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Canonical Allele Identifier:
CA11026464
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.118118540G>T
GRCh37
chr2:g.118876116G>T
Linked Data - Sequence & Population
gnomAD v2:
2:118876116 G / T
gnomAD v3:
2:118118540 G / T
gnomAD v4:
chr2-118118540-G-T
Joint Max Group AF
0.15973474 (AFR)
Genomes Max Group AF
0.15973474 (AFR)
Linked Data - NCBI & NCI
dbSNP:
11673900
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.118118540G>T , CM000664.2:g.118118540G>T
GRCh38
NC_000002.11:g.118876116G>T , CM000664.1:g.118876116G>T
GRCh37
NC_000002.10:g.118592586G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'