Canonical Allele Identifier: CA227398472

Gene: WTAPP1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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