Canonical Allele Identifier: CA236626584
Gene: WNT10B HGNC NCBI

Linked Data

dbSNP Id: rs535698374

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48966213C>T , CM000674.2:g.48966213C>T GRCh38
NC_000012.11:g.49359996C>T , CM000674.1:g.49359996C>T GRCh37
NC_000012.10:g.47646263C>T NCBI36
NG_023347.1:g.10646G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000301061.9:c.1052G>A MANE Select ENSP00000301061.4:p.Arg351His
ENST00000301061.8:c.1052G>A ENSP00000301061.4:p.Arg351His
ENST00000403957.5:c.*334G>A ENSP00000385980.1:n.*334G>A
ENST00000407467.5:c.*334G>A ENSP00000384691.1:n.*334G>A
NM_003394.3:c.1052G>A NP_003385.2:p.Arg351His
XM_011538721.1:c.686G>A XP_011537023.1:p.Arg229His
XM_011538722.1:c.686G>A XP_011537024.1:p.Arg229His
XM_011538724.1:c.*330G>A XP_011537026.1:n.*330G>A
XM_017019919.1:c.686G>A XP_016875408.1:p.Arg229His
XM_024449179.1:c.686G>A XP_024304947.1:p.Arg229His
NM_003394.4:c.1052G>A MANE Select NP_003385.2:p.Arg351His