Canonical Allele Identifier: CA670868049

Gene: WTAPP1

Linked Data

• dbSNP Id: rs1206786885
• MyVariant Identifiers: chr11:g.102656424A>C (hg19) ; chr11:g.102785693A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102785693A>C , CM000673.2:g.102785693A>C	GRCh38
NC_000011.9:g.102656424A>C , CM000673.1:g.102656424A>C	GRCh37
NC_000011.8:g.102161634A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000371455.7:n.325-12331A>C
ENST00000525739.6:n.389+1629A>C
ENST00000544704.1:n.344+1629A>C
NR_038390.1:n.389+1629A>C