Canonical Allele Identifier: CA227378220
Gene: WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs539498493
gnomAD v2: 11-102680181-A-G
gnomAD v3: 11-102809450-A-G
gnomAD v4: 11-102809450-A-G
MyVariant Identifiers: chr11:g.102680181A>G (hg19) chr11:g.102809450A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102809450A>G , CM000673.2:g.102809450A>G GRCh38
NC_000011.9:g.102680181A>G , CM000673.1:g.102680181A>G GRCh37
NC_000011.8:g.102185391A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371455.7:n.423+11328A>G
ENST00000525739.6:n.682+11328A>G
ENST00000544704.1:n.443+11328A>G
NR_038390.1:n.682+11328A>G
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