Canonical Allele Identifier: CA13427592
Gene: WTAPP1 HGNC NCBI
gnomAD v2:
11:102703628 A / G
gnomAD v3:
11:102832897 A / G
gnomAD v4:
chr11-102832897-A-G
Joint Max Group AF 0.6775348 (SAS)
Genomes Max Group AF 0.6775348 (SAS)
Exomes Max Group AF 0.113859 (NFE)
dbSNP:
635746
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102832897A>G , CM000673.2:g.102832897A>G GRCh38
NC_000011.9:g.102703628A>G , CM000673.1:g.102703628A>G GRCh37
NC_000011.8:g.102208838A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000525739.6:n.2191A>G
NR_038390.1:n.2191A>G
Search 100 bp 5'
Search 100 bp 3'