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Canonical Allele Identifier:
CA11001492
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.15589696T>G
GRCh37
chr2:g.15729820T>G
Linked Data - Sequence & Population
gnomAD v2:
2:15729820 T / G
gnomAD v3:
2:15589696 T / G
gnomAD v4:
chr2-15589696-T-G
Joint Max Group AF
0.47860578 (AFR)
Genomes Max Group AF
0.47860578 (AFR)
Linked Data - NCBI & NCI
dbSNP:
3755132
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.15589696T>G , CM000664.2:g.15589696T>G
GRCh38
NC_000002.11:g.15729820T>G , CM000664.1:g.15729820T>G
GRCh37
NC_000002.10:g.15647271T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'