Canonical Allele Identifier: CA384678851

Gene: WNT10B

Linked Data

• ClinVar Variation Id: 545118
• ClinVar RCV Id: RCV000656339
• dbSNP Id: rs1163162816
• MyVariant Identifiers: chr12:g.49362103C>G (hg19) ; chr12:g.48968320C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48968320C>G , CM000674.2:g.48968320C>G	GRCh38
NC_000012.11:g.49362103C>G , CM000674.1:g.49362103C>G	GRCh37
NC_000012.10:g.47648370C>G	NCBI36
NG_023347.1:g.8539G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301061.9:c.338-1G>C MANE Select	ENSP00000301061.4:n.338-1G>C
ENST00000301061.8:c.338-1G>C	ENSP00000301061.4:n.338-1G>C
ENST00000403957.5:c.338-1G>C	ENSP00000385980.1:n.338-1G>C
ENST00000407467.5:c.338-1G>C	ENSP00000384691.1:n.338-1G>C
ENST00000413630.1:c.373-1G>C	ENSP00000398473.1:n.373-1G>C
NM_003394.3:c.338-1G>C	NP_003385.2:n.338-1G>C
XM_011538721.1:c.-29-1G>C	XP_011537023.1:n.-29-1G>C
XM_011538722.1:c.-29-1G>C	XP_011537024.1:n.-29-1G>C
XM_011538723.1:c.338-1G>C	XP_011537025.1:n.338-1G>C
XM_011538724.1:c.338-1G>C	XP_011537026.1:n.338-1G>C
XM_017019919.1:c.-29-1G>C	XP_016875408.1:n.-29-1G>C
XM_024449179.1:c.-29-1G>C	XP_024304947.1:n.-29-1G>C
NM_003394.4:c.338-1G>C MANE Select	NP_003385.2:n.338-1G>C