Canonical Allele Identifier: CA2034911568
Gene: WNT10B HGNC NCBI

Linked Data

dbSNP Id: rs1940719966
gnomAD v4: 12-48965803-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48965803C>T , CM000674.2:g.48965803C>T GRCh38
NC_000012.11:g.49359586C>T , CM000674.1:g.49359586C>T GRCh37
NC_000012.10:g.47645853C>T NCBI36
NG_023347.1:g.11056G>A

Transcript Alleles

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