Canonical Allele Identifier: CA601245746
Gene: WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1200024607
gnomAD v2: 11-102656578-G-C
gnomAD v3: 11-102785847-G-C
gnomAD v4: 11-102785847-G-C
MyVariant Identifiers: chr11:g.102656578G>C (hg19) chr11:g.102785847G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102785847G>C , CM000673.2:g.102785847G>C GRCh38
NC_000011.9:g.102656578G>C , CM000673.1:g.102656578G>C GRCh37
NC_000011.8:g.102161788G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371455.7:n.325-12177G>C
ENST00000525739.6:n.389+1783G>C
ENST00000544704.1:n.344+1783G>C
NR_038390.1:n.389+1783G>C
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