Canonical Allele Identifier: CA479703722

Gene: WNT10B

Linked Data

• dbSNP Id: rs1592249581
• MyVariant Identifiers: chr12:g.49359995A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48966212A>C , CM000674.2:g.48966212A>C	GRCh38
NC_000012.11:g.49359995A>C , CM000674.1:g.49359995A>C	GRCh37
NC_000012.10:g.47646262A>C	NCBI36
NG_023347.1:g.10647T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000301061.9:c.1053T>G MANE Select	ENSP00000301061.4:p.Arg351=
ENST00000301061.8:c.1053T>G	ENSP00000301061.4:p.Arg351=
ENST00000403957.5:c.*335T>G	ENSP00000385980.1:n.*335T>G
ENST00000407467.5:c.*335T>G	ENSP00000384691.1:n.*335T>G
NM_003394.3:c.1053T>G	NP_003385.2:p.Arg351=
XM_011538721.1:c.687T>G	XP_011537023.1:p.Arg229=
XM_011538722.1:c.687T>G	XP_011537024.1:p.Arg229=
XM_011538724.1:c.*331T>G	XP_011537026.1:n.*331T>G
XM_017019919.1:c.687T>G	XP_016875408.1:p.Arg229=
XM_024449179.1:c.687T>G	XP_024304947.1:p.Arg229=
NM_003394.4:c.1053T>G MANE Select	NP_003385.2:p.Arg351=