Canonical Allele Identifier: CA384670717

Gene: WNT10B

Linked Data

• MyVariant Identifiers: chr12:g.49359886A>T (hg19) ; chr12:g.48966103A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48966103A>T , CM000674.2:g.48966103A>T	GRCh38
NC_000012.11:g.49359886A>T , CM000674.1:g.49359886A>T	GRCh37
NC_000012.10:g.47646153A>T	NCBI36
NG_023347.1:g.10756T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301061.9:c.1162T>A MANE Select	ENSP00000301061.4:p.Cys388Ser
ENST00000301061.8:c.1162T>A	ENSP00000301061.4:p.Cys388Ser
ENST00000403957.5:c.*444T>A	ENSP00000385980.1:n.*444T>A
ENST00000407467.5:c.*444T>A	ENSP00000384691.1:n.*444T>A
NM_003394.3:c.1162T>A	NP_003385.2:p.Cys388Ser
XM_011538721.1:c.796T>A	XP_011537023.1:p.Cys266Ser
XM_011538722.1:c.796T>A	XP_011537024.1:p.Cys266Ser
XM_017019919.1:c.796T>A	XP_016875408.1:p.Cys266Ser
XM_024449179.1:c.796T>A	XP_024304947.1:p.Cys266Ser
NM_003394.4:c.1162T>A MANE Select	NP_003385.2:p.Cys388Ser