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Canonical Allele Identifier:
CA16155014
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr3:g.114229128T>C
GRCh37
chr3:g.113947975T>C
Linked Data - Sequence & Population
gnomAD v2:
3:113947975 T / C
gnomAD v3:
3:114229128 T / C
gnomAD v4:
chr3-114229128-T-C
Joint Max Group AF
0.31254096 (EAS)
Genomes Max Group AF
0.31254096 (EAS)
Linked Data - NCBI & NCI
dbSNP:
7620754
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.114229128T>C , CM000665.2:g.114229128T>C
GRCh38
NC_000003.11:g.113947975T>C , CM000665.1:g.113947975T>C
GRCh37
NC_000003.10:g.115430665T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_001740856.1:n.161-4214T>C
Search 100 bp 5'
Search 100 bp 3'