Canonical Allele Identifier: CA384673501

Gene: WNT10B

Linked Data

• dbSNP Id: rs766021478
• gnomAD v4: 12-48966479-C-G
• MyVariant Identifiers: chr12:g.49360262C>G (hg19) ; chr12:g.48966479C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48966479C>G , CM000674.2:g.48966479C>G	GRCh38
NC_000012.11:g.49360262C>G , CM000674.1:g.49360262C>G	GRCh37
NC_000012.10:g.47646529C>G	NCBI36
NG_023347.1:g.10380G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000301061.9:c.786G>C MANE Select	ENSP00000301061.4:p.Trp262Cys
ENST00000301061.8:c.786G>C	ENSP00000301061.4:p.Trp262Cys
ENST00000403957.5:c.*68G>C	ENSP00000385980.1:n.*68G>C
ENST00000407467.5:c.*68G>C	ENSP00000384691.1:n.*68G>C
NM_003394.3:c.786G>C	NP_003385.2:p.Trp262Cys
XM_011538721.1:c.420G>C	XP_011537023.1:p.Trp140Cys
XM_011538722.1:c.420G>C	XP_011537024.1:p.Trp140Cys
XM_011538723.1:c.*68G>C	XP_011537025.1:n.*68G>C
XM_011538724.1:c.*64G>C	XP_011537026.1:n.*64G>C
XM_017019919.1:c.420G>C	XP_016875408.1:p.Trp140Cys
XM_024449179.1:c.420G>C	XP_024304947.1:p.Trp140Cys
NM_003394.4:c.786G>C MANE Select	NP_003385.2:p.Trp262Cys