Canonical Allele Identifier: CA479703451

Gene: WNT10B

Linked Data

• dbSNP Id: rs2137610621
• MyVariant Identifiers: chr12:g.49359890A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48966107A>G , CM000674.2:g.48966107A>G	GRCh38
NC_000012.11:g.49359890A>G , CM000674.1:g.49359890A>G	GRCh37
NC_000012.10:g.47646157A>G	NCBI36
NG_023347.1:g.10752T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000301061.9:c.1158T>C MANE Select	ENSP00000301061.4:p.Asn386=
ENST00000301061.8:c.1158T>C	ENSP00000301061.4:p.Asn386=
ENST00000403957.5:c.*440T>C	ENSP00000385980.1:n.*440T>C
ENST00000407467.5:c.*440T>C	ENSP00000384691.1:n.*440T>C
NM_003394.3:c.1158T>C	NP_003385.2:p.Asn386=
XM_011538721.1:c.792T>C	XP_011537023.1:p.Asn264=
XM_011538722.1:c.792T>C	XP_011537024.1:p.Asn264=
XM_017019919.1:c.792T>C	XP_016875408.1:p.Asn264=
XM_024449179.1:c.792T>C	XP_024304947.1:p.Asn264=
NM_003394.4:c.1158T>C MANE Select	NP_003385.2:p.Asn386=