Canonical Allele Identifier: CA13555058
Gene: WTAPP1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1939008

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102785692G>A , CM000673.2:g.102785692G>A GRCh38
NC_000011.9:g.102656423G>A , CM000673.1:g.102656423G>A GRCh37
NC_000011.8:g.102161633G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038390.1:n.389+1628G>A
ENST00000371455.7:n.325-12332G>A
ENST00000525739.6:n.389+1628G>A
ENST00000544704.1:n.344+1628G>A