Canonical Allele Identifier: CA2602013046
Gene: WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs2134379226
gnomAD v3: 11-102809500-T-G
gnomAD v4: 11-102809500-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102809500T>G , CM000673.2:g.102809500T>G GRCh38
NC_000011.9:g.102680231T>G , CM000673.1:g.102680231T>G GRCh37
NC_000011.8:g.102185441T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371455.7:n.423+11378T>G
ENST00000525739.6:n.682+11378T>G
ENST00000544704.1:n.443+11378T>G
NR_038390.1:n.682+11378T>G
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