Canonical Allele Identifier: CA16132435
Gene:
MyVariant.info:
GRCh38 chr3:g.856978C>T
GRCh37 chr3:g.898661C>T
gnomAD v2:
3:898661 C / T
gnomAD v3:
3:856978 C / T
gnomAD v4:
chr3-856978-C-T
Joint Max Group AF 0.53357586 (EAS)
Genomes Max Group AF 0.53357586 (EAS)
dbSNP:
35964523
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.856978C>T , CM000665.2:g.856978C>T GRCh38
NC_000003.11:g.898661C>T , CM000665.1:g.898661C>T GRCh37
NC_000003.10:g.873661C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001740584.1:n.1837C>T
Search 100 bp 5'
Search 100 bp 3'