Canonical Allele Identifier: CA479703719

Gene: WNT10B

Linked Data

• MyVariant Identifiers: chr12:g.49359992C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48966209C>T , CM000674.2:g.48966209C>T	GRCh38
NC_000012.11:g.49359992C>T , CM000674.1:g.49359992C>T	GRCh37
NC_000012.10:g.47646259C>T	NCBI36
NG_023347.1:g.10650G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000301061.9:c.1056G>A MANE Select	ENSP00000301061.4:p.Gly352=
ENST00000301061.8:c.1056G>A	ENSP00000301061.4:p.Gly352=
ENST00000403957.5:c.*338G>A	ENSP00000385980.1:n.*338G>A
ENST00000407467.5:c.*338G>A	ENSP00000384691.1:n.*338G>A
NM_003394.3:c.1056G>A	NP_003385.2:p.Gly352=
XM_011538721.1:c.690G>A	XP_011537023.1:p.Gly230=
XM_011538722.1:c.690G>A	XP_011537024.1:p.Gly230=
XM_011538724.1:c.*334G>A	XP_011537026.1:n.*334G>A
XM_017019919.1:c.690G>A	XP_016875408.1:p.Gly230=
XM_024449179.1:c.690G>A	XP_024304947.1:p.Gly230=
NM_003394.4:c.1056G>A MANE Select	NP_003385.2:p.Gly352=