Canonical Allele Identifier: CA670876288
Gene: WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1349453941
gnomAD v3: 11-102798299-C-A
gnomAD v4: 11-102798299-C-A
MyVariant Identifiers: chr11:g.102669030C>A (hg19) chr11:g.102798299C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102798299C>A , CM000673.2:g.102798299C>A GRCh38
NC_000011.9:g.102669030C>A , CM000673.1:g.102669030C>A GRCh37
NC_000011.8:g.102174240C>A NCBI36
NG_011740.1:g.4937G>T
NG_011740.2:g.4937G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371455.7:n.423+177C>A
ENST00000525739.6:n.682+177C>A
ENST00000544704.1:n.443+177C>A
NR_038390.1:n.682+177C>A
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