Canonical Allele Identifier: CA227368104
Gene: WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs888636969
gnomAD v3: 11-102798570-G-A
gnomAD v4: 11-102798570-G-A
MyVariant Identifiers: chr11:g.102669301G>A (hg19) chr11:g.102798570G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102798570G>A , CM000673.2:g.102798570G>A GRCh38
NC_000011.9:g.102669301G>A , CM000673.1:g.102669301G>A GRCh37
NC_000011.8:g.102174511G>A NCBI36
NG_011740.1:g.4666C>T
NG_011740.2:g.4666C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371455.7:n.423+448G>A
ENST00000525739.6:n.682+448G>A
ENST00000544704.1:n.443+448G>A
NR_038390.1:n.682+448G>A
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