Canonical Allele Identifier: CA601245744
Gene: WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1207143216
gnomAD v2: 11-102656525-T-G
gnomAD v3: 11-102785794-T-G
gnomAD v4: 11-102785794-T-G
MyVariant Identifiers: chr11:g.102656525T>G (hg19) chr11:g.102785794T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102785794T>G , CM000673.2:g.102785794T>G GRCh38
NC_000011.9:g.102656525T>G , CM000673.1:g.102656525T>G GRCh37
NC_000011.8:g.102161735T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371455.7:n.325-12230T>G
ENST00000525739.6:n.389+1730T>G
ENST00000544704.1:n.344+1730T>G
NR_038390.1:n.389+1730T>G
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