Canonical Allele Identifier: CA479703729

Gene: WNT10B

Linked Data

• MyVariant Identifiers: chr12:g.49359998G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48966215G>C , CM000674.2:g.48966215G>C	GRCh38
NC_000012.11:g.49359998G>C , CM000674.1:g.49359998G>C	GRCh37
NC_000012.10:g.47646265G>C	NCBI36
NG_023347.1:g.10644C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000301061.9:c.1050C>G MANE Select	ENSP00000301061.4:p.Gly350=
ENST00000301061.8:c.1050C>G	ENSP00000301061.4:p.Gly350=
ENST00000403957.5:c.*332C>G	ENSP00000385980.1:n.*332C>G
ENST00000407467.5:c.*332C>G	ENSP00000384691.1:n.*332C>G
NM_003394.3:c.1050C>G	NP_003385.2:p.Gly350=
XM_011538721.1:c.684C>G	XP_011537023.1:p.Gly228=
XM_011538722.1:c.684C>G	XP_011537024.1:p.Gly228=
XM_011538724.1:c.*328C>G	XP_011537026.1:n.*328C>G
XM_017019919.1:c.684C>G	XP_016875408.1:p.Gly228=
XM_024449179.1:c.684C>G	XP_024304947.1:p.Gly228=
NM_003394.4:c.1050C>G MANE Select	NP_003385.2:p.Gly350=