Canonical Allele Identifier: CA476575298

Gene: WTAPP1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102832897A>C , CM000673.2:g.102832897A>C	GRCh38
NC_000011.9:g.102703628A>C , CM000673.1:g.102703628A>C	GRCh37
NC_000011.8:g.102208838A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525739.6:n.2191A>C
NR_038390.1:n.2191A>C