Canonical Allele Identifier: CA1996247092
Gene: WTAPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102809407A= , CM000673.2:g.102809407A= GRCh38
NC_000011.9:g.102680138A= , CM000673.1:g.102680138A= GRCh37
NC_000011.8:g.102185348A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371455.7:n.423+11285A=
ENST00000525739.6:n.682+11285A=
ENST00000544704.1:n.443+11285A=
NR_038390.1:n.682+11285A=