Canonical Allele Identifier: CA227368188
Gene: WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs896939560

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102798602G>C , CM000673.2:g.102798602G>C GRCh38
NC_000011.9:g.102669333G>C , CM000673.1:g.102669333G>C GRCh37
NC_000011.8:g.102174543G>C NCBI36
NG_011740.1:g.4634C>G
NG_011740.2:g.4634C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371455.7:n.423+480G>C
ENST00000525739.6:n.682+480G>C
ENST00000544704.1:n.443+480G>C
NR_038390.1:n.682+480G>C