Canonical Allele Identifier: CA601246174
Gene: WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1185074453

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102798644T>C , CM000673.2:g.102798644T>C GRCh38
NC_000011.9:g.102669375T>C , CM000673.1:g.102669375T>C GRCh37
NC_000011.8:g.102174585T>C NCBI36
NG_011740.1:g.4592A>G
NG_011740.2:g.4592A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371455.7:n.423+522T>C
ENST00000525739.6:n.682+522T>C
ENST00000544704.1:n.443+522T>C
NR_038390.1:n.682+522T>C