Canonical Allele Identifier: CA384671277

Gene: WNT10B

Linked Data

• ClinVar Variation Id: 452097
• ClinVar RCV Id: RCV000520692
• dbSNP Id: rs772141128
• MyVariant Identifiers: chr12:g.49359961G>C (hg19) ; chr12:g.48966178G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48966178G>C , CM000674.2:g.48966178G>C	GRCh38
NC_000012.11:g.49359961G>C , CM000674.1:g.49359961G>C	GRCh37
NC_000012.10:g.47646228G>C	NCBI36
NG_023347.1:g.10681C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301061.9:c.1087C>G MANE Select	ENSP00000301061.4:p.Arg363Gly
ENST00000301061.8:c.1087C>G	ENSP00000301061.4:p.Arg363Gly
ENST00000403957.5:c.*369C>G	ENSP00000385980.1:n.*369C>G
ENST00000407467.5:c.*369C>G	ENSP00000384691.1:n.*369C>G
NM_003394.3:c.1087C>G	NP_003385.2:p.Arg363Gly
XM_011538721.1:c.721C>G	XP_011537023.1:p.Arg241Gly
XM_011538722.1:c.721C>G	XP_011537024.1:p.Arg241Gly
XM_011538724.1:c.*365C>G	XP_011537026.1:n.*365C>G
XM_017019919.1:c.721C>G	XP_016875408.1:p.Arg241Gly
XM_024449179.1:c.721C>G	XP_024304947.1:p.Arg241Gly
NM_003394.4:c.1087C>G MANE Select	NP_003385.2:p.Arg363Gly