Canonical Allele Identifier: CA670868125
Gene: WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1277975964
gnomAD v3: 11-102785835-T-C
gnomAD v4: 11-102785835-T-C
MyVariant Identifiers: chr11:g.102656566T>C (hg19) chr11:g.102785835T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102785835T>C , CM000673.2:g.102785835T>C GRCh38
NC_000011.9:g.102656566T>C , CM000673.1:g.102656566T>C GRCh37
NC_000011.8:g.102161776T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371455.7:n.325-12189T>C
ENST00000525739.6:n.389+1771T>C
ENST00000544704.1:n.344+1771T>C
NR_038390.1:n.389+1771T>C
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