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Canonical Allele Identifier:
CA11130696
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.160928658C>T
GRCh37
chr2:g.161785169C>T
Linked Data - Sequence & Population
gnomAD v2:
2:161785169 C / T
gnomAD v3:
2:160928658 C / T
gnomAD v4:
chr2-160928658-C-T
Joint Max Group AF
0.31459375 (EAS)
Genomes Max Group AF
0.31459375 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1829975
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.160928658C>T , CM000664.2:g.160928658C>T
GRCh38
NC_000002.11:g.161785169C>T , CM000664.1:g.161785169C>T
GRCh37
NC_000002.10:g.161493415C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'