Canonical Allele Identifier: CA1996247115
Gene: WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1858459203

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102809466A>C , CM000673.2:g.102809466A>C GRCh38
NC_000011.9:g.102680197A>C , CM000673.1:g.102680197A>C GRCh37
NC_000011.8:g.102185407A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371455.7:n.423+11344A>C
ENST00000525739.6:n.682+11344A>C
ENST00000544704.1:n.443+11344A>C
NR_038390.1:n.682+11344A>C