Canonical Allele Identifier: CA11404988

Gene: TWF2

Linked Data

• dbSNP Id: rs7618915
• gnomAD v2: 3-52279594-G-A
• gnomAD v3: 3-52245578-G-A
• gnomAD v4: 3-52245578-G-A
• MyVariant Identifiers: chr3:g.52279594G>A (hg19) ; chr3:g.52245578G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52245578G>A , CM000665.2:g.52245578G>A	GRCh38
NC_000003.11:g.52279594G>A , CM000665.1:g.52279594G>A	GRCh37
NC_000003.10:g.52254634G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000679296.1:c.-270+1101C>T	ENSP00000504576.1:n.-270+1101C>T