Canonical Allele Identifier: CA670876462
Gene: WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1458061256
gnomAD v3: 11-102798586-T-A
gnomAD v4: 11-102798586-T-A
MyVariant Identifiers: chr11:g.102669317T>A (hg19) chr11:g.102798586T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102798586T>A , CM000673.2:g.102798586T>A GRCh38
NC_000011.9:g.102669317T>A , CM000673.1:g.102669317T>A GRCh37
NC_000011.8:g.102174527T>A NCBI36
NG_011740.1:g.4650A>T
NG_011740.2:g.4650A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371455.7:n.423+464T>A
ENST00000525739.6:n.682+464T>A
ENST00000544704.1:n.443+464T>A
NR_038390.1:n.682+464T>A
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