Canonical Allele Identifier: CA2618596023
Gene: WNT10B HGNC NCBI

Linked Data

gnomAD v4: 12-48965982-T-TA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48965983dup , CM000674.2:g.48965983dup GRCh38
NC_000012.11:g.49359766dup , CM000674.1:g.49359766dup GRCh37
NC_000012.10:g.47646033dup NCBI36
NG_023347.1:g.10876dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000301061.9:c.*112dup MANE Select ENSP00000301061.4:n.*112dup
ENST00000301061.8:c.*112dup ENSP00000301061.4:n.*112dup
ENST00000403957.5:c.*564dup ENSP00000385980.1:n.*564dup
ENST00000407467.5:c.*564dup ENSP00000384691.1:n.*564dup
NM_003394.3:c.*112dup NP_003385.2:n.*112dup
XM_011538721.1:c.*112dup XP_011537023.1:n.*112dup
XM_011538722.1:c.*112dup XP_011537024.1:n.*112dup
XM_017019919.1:c.*112dup XP_016875408.1:n.*112dup
XM_024449179.1:c.*112dup XP_024304947.1:n.*112dup
NM_003394.4:c.*112dup MANE Select NP_003385.2:n.*112dup
Search 100 bp 5'
Search 100 bp 3'