Canonical Allele Identifier: CA601245740
Gene: WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1408902331
gnomAD v2: 11-102656327-G-T
gnomAD v3: 11-102785596-G-T
gnomAD v4: 11-102785596-G-T
MyVariant Identifiers: chr11:g.102656327G>T (hg19) chr11:g.102785596G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102785596G>T , CM000673.2:g.102785596G>T GRCh38
NC_000011.9:g.102656327G>T , CM000673.1:g.102656327G>T GRCh37
NC_000011.8:g.102161537G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371455.7:n.325-12428G>T
ENST00000525739.6:n.389+1532G>T
ENST00000544704.1:n.344+1532G>T
NR_038390.1:n.389+1532G>T
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