Canonical Allele Identifier: CA2724644912
Gene: WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1858264198

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102798314C>T , CM000673.2:g.102798314C>T GRCh38
NC_000011.9:g.102669045C>T , CM000673.1:g.102669045C>T GRCh37
NC_000011.8:g.102174255C>T NCBI36
NG_011740.1:g.4922G>A
NG_011740.2:g.4922G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371455.7:n.423+192C>T
ENST00000525739.6:n.682+192C>T
ENST00000544704.1:n.443+192C>T
NR_038390.1:n.682+192C>T