Canonical Allele Identifier: CA227398472
Gene: WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs17099545

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