Canonical Allele Identifier: CA2724608215
Gene: WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1184939710

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102798608C>T , CM000673.2:g.102798608C>T GRCh38
NC_000011.9:g.102669339C>T , CM000673.1:g.102669339C>T GRCh37
NC_000011.8:g.102174549C>T NCBI36
NG_011740.1:g.4628G>A
NG_011740.2:g.4628G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371455.7:n.423+486C>T
ENST00000525739.6:n.682+486C>T
ENST00000544704.1:n.443+486C>T
NR_038390.1:n.682+486C>T