Canonical Allele Identifier: CA3182657314
Gene: WTAPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102761462A= , CM000673.2:g.102761462A= GRCh38
NC_000011.9:g.102632193A= , CM000673.1:g.102632193A= GRCh37
NC_000011.8:g.102137403A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000371455.7:n.324+10036A=