Canonical Allele Identifier: CA941635167
Gene: WTAPP1 HGNC NCBI
gnomAD v3:
11:102809235 G / A
gnomAD v4:
chr11-102809235-G-A
Joint Max Group AF 0.00000801 (AFR)
Genomes Max Group AF 0.00000801 (AFR)
dbSNP:
12289128
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102809235G>A , CM000673.2:g.102809235G>A GRCh38
NC_000011.9:g.102679966G>A , CM000673.1:g.102679966G>A GRCh37
NC_000011.8:g.102185176G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000371455.7:n.423+11113G>A
ENST00000525739.6:n.682+11113G>A
ENST00000544704.1:n.443+11113G>A
NR_038390.1:n.682+11113G>A
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