Canonical Allele Identifier: CA227356536
Gene: WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs145887391

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102785723A>G , CM000673.2:g.102785723A>G GRCh38
NC_000011.9:g.102656454A>G , CM000673.1:g.102656454A>G GRCh37
NC_000011.8:g.102161664A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371455.7:n.325-12301A>G
ENST00000525739.6:n.389+1659A>G
ENST00000544704.1:n.344+1659A>G
NR_038390.1:n.389+1659A>G