Canonical Allele Identifier: CA2618595818
Gene: WNT10B HGNC NCBI

Linked Data

gnomAD v4: 12-48965802-GC-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48965803del , CM000674.2:g.48965803del GRCh38
NC_000012.11:g.49359586del , CM000674.1:g.49359586del GRCh37
NC_000012.10:g.47645853del NCBI36
NG_023347.1:g.11056del

Transcript Alleles

HGVS Amino-acid Change
ENST00000301061.9:c.*292del MANE Select ENSP00000301061.4:n.*292del
ENST00000301061.8:c.*292del ENSP00000301061.4:n.*292del
ENST00000403957.5:c.*744del ENSP00000385980.1:n.*744del
ENST00000407467.5:c.*744del ENSP00000384691.1:n.*744del
NM_003394.3:c.*292del NP_003385.2:n.*292del
XM_011538721.1:c.*292del XP_011537023.1:n.*292del
XM_011538722.1:c.*292del XP_011537024.1:n.*292del
XM_017019919.1:c.*292del XP_016875408.1:n.*292del
XM_024449179.1:c.*292del XP_024304947.1:n.*292del
NM_003394.4:c.*292del MANE Select NP_003385.2:n.*292del
Search 100 bp 5'
Search 100 bp 3'