Canonical Allele Identifier: CA601246566
Gene: WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1301854852
gnomAD v2: 11-102680171-T-A
gnomAD v3: 11-102809440-T-A
gnomAD v4: 11-102809440-T-A
MyVariant Identifiers: chr11:g.102680171T>A (hg19) chr11:g.102809440T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102809440T>A , CM000673.2:g.102809440T>A GRCh38
NC_000011.9:g.102680171T>A , CM000673.1:g.102680171T>A GRCh37
NC_000011.8:g.102185381T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371455.7:n.423+11318T>A
ENST00000525739.6:n.682+11318T>A
ENST00000544704.1:n.443+11318T>A
NR_038390.1:n.682+11318T>A
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