Canonical Allele Identifier: CA227367911
Gene: WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs936784476
gnomAD v2: 11-102669022-A-T
gnomAD v3: 11-102798291-A-T
gnomAD v4: 11-102798291-A-T
MyVariant Identifiers: chr11:g.102669022A>T (hg19) chr11:g.102798291A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102798291A>T , CM000673.2:g.102798291A>T GRCh38
NC_000011.9:g.102669022A>T , CM000673.1:g.102669022A>T GRCh37
NC_000011.8:g.102174232A>T NCBI36
NG_011740.1:g.4945T>A
NG_011740.2:g.4945T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371455.7:n.423+169A>T
ENST00000525739.6:n.682+169A>T
ENST00000544704.1:n.443+169A>T
NR_038390.1:n.682+169A>T
Search 100 bp 5'
Search 100 bp 3'