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Canonical Allele Identifier:
CA14629967
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.77926067T>C
GRCh37
chr18:g.75638023T>C
Linked Data - Sequence & Population
gnomAD v2:
18:75638023 T / C
gnomAD v3:
18:77926067 T / C
gnomAD v4:
chr18-77926067-T-C
Joint Max Group AF
0.65445877 (EAS)
Genomes Max Group AF
0.65445877 (EAS)
Linked Data - NCBI & NCI
dbSNP:
12455580
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.77926067T>C , CM000680.2:g.77926067T>C
GRCh38
NC_000018.9:g.75638023T>C , CM000680.1:g.75638023T>C
GRCh37
NC_000018.8:g.73767011T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'