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Canonical Allele Identifier:
CA11018980
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr2:g.79099089T>C
GRCh37
chr2:g.79326215T>C
Linked Data - Sequence & Population
gnomAD v2:
2:79326215 T / C
gnomAD v3:
2:79099089 T / C
gnomAD v4:
chr2-79099089-T-C
Joint Max Group AF
0.42769764 (SAS)
Genomes Max Group AF
0.42769764 (SAS)
Linked Data - NCBI & NCI
dbSNP:
283895
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.79099089T>C , CM000664.2:g.79099089T>C
GRCh38
NC_000002.11:g.79326215T>C , CM000664.1:g.79326215T>C
GRCh37
NC_000002.10:g.79179723T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'