Canonical Allele Identifier: CA227356530
Gene: WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs567841953

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102785712A>G , CM000673.2:g.102785712A>G GRCh38
NC_000011.9:g.102656443A>G , CM000673.1:g.102656443A>G GRCh37
NC_000011.8:g.102161653A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371455.7:n.325-12312A>G
ENST00000525739.6:n.389+1648A>G
ENST00000544704.1:n.344+1648A>G
NR_038390.1:n.389+1648A>G