Canonical Allele Identifier: CA2618595970
Gene: WNT10B HGNC NCBI

Linked Data

gnomAD v4: 12-48965939-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48965939G>T , CM000674.2:g.48965939G>T GRCh38
NC_000012.11:g.49359722G>T , CM000674.1:g.49359722G>T GRCh37
NC_000012.10:g.47645989G>T NCBI36
NG_023347.1:g.10920C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301061.9:c.*156C>A MANE Select ENSP00000301061.4:n.*156C>A
ENST00000301061.8:c.*156C>A ENSP00000301061.4:n.*156C>A
ENST00000403957.5:c.*608C>A ENSP00000385980.1:n.*608C>A
ENST00000407467.5:c.*608C>A ENSP00000384691.1:n.*608C>A
NM_003394.3:c.*156C>A NP_003385.2:n.*156C>A
XM_011538721.1:c.*156C>A XP_011537023.1:n.*156C>A
XM_011538722.1:c.*156C>A XP_011537024.1:n.*156C>A
XM_017019919.1:c.*156C>A XP_016875408.1:n.*156C>A
XM_024449179.1:c.*156C>A XP_024304947.1:n.*156C>A
NM_003394.4:c.*156C>A MANE Select NP_003385.2:n.*156C>A
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