Canonical Allele Identifier: CA670868082

Gene: WTAPP1

Linked Data

• dbSNP Id: rs1381009730
• MyVariant Identifiers: chr11:g.102656499C>T (hg19) ; chr11:g.102785768C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102785768C>T , CM000673.2:g.102785768C>T	GRCh38
NC_000011.9:g.102656499C>T , CM000673.1:g.102656499C>T	GRCh37
NC_000011.8:g.102161709C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000371455.7:n.325-12256C>T
ENST00000525739.6:n.389+1704C>T
ENST00000544704.1:n.344+1704C>T
NR_038390.1:n.389+1704C>T