Canonical Allele Identifier: CA384671644

Gene: WNT10B

Linked Data

• dbSNP Id: rs1165695871
• gnomAD v2: 12-49360003-A-G
• gnomAD v4: 12-48966220-A-G
• MyVariant Identifiers: chr12:g.49360003A>G (hg19) ; chr12:g.48966220A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48966220A>G , CM000674.2:g.48966220A>G	GRCh38
NC_000012.11:g.49360003A>G , CM000674.1:g.49360003A>G	GRCh37
NC_000012.10:g.47646270A>G	NCBI36
NG_023347.1:g.10639T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000301061.9:c.1045T>C MANE Select	ENSP00000301061.4:p.Cys349Arg
ENST00000301061.8:c.1045T>C	ENSP00000301061.4:p.Cys349Arg
ENST00000403957.5:c.*327T>C	ENSP00000385980.1:n.*327T>C
ENST00000407467.5:c.*327T>C	ENSP00000384691.1:n.*327T>C
NM_003394.3:c.1045T>C	NP_003385.2:p.Cys349Arg
XM_011538721.1:c.679T>C	XP_011537023.1:p.Cys227Arg
XM_011538722.1:c.679T>C	XP_011537024.1:p.Cys227Arg
XM_011538724.1:c.*323T>C	XP_011537026.1:n.*323T>C
XM_017019919.1:c.679T>C	XP_016875408.1:p.Cys227Arg
XM_024449179.1:c.679T>C	XP_024304947.1:p.Cys227Arg
NM_003394.4:c.1045T>C MANE Select	NP_003385.2:p.Cys349Arg