Canonical Allele Identifier: CA384670683

Gene: WNT10B

Linked Data

• MyVariant Identifiers: chr12:g.49359882T>G (hg19) ; chr12:g.48966099T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48966099T>G , CM000674.2:g.48966099T>G	GRCh38
NC_000012.11:g.49359882T>G , CM000674.1:g.49359882T>G	GRCh37
NC_000012.10:g.47646149T>G	NCBI36
NG_023347.1:g.10760A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301061.9:c.1166A>C MANE Select	ENSP00000301061.4:p.Lys389Thr
ENST00000301061.8:c.1166A>C	ENSP00000301061.4:p.Lys389Thr
ENST00000403957.5:c.*448A>C	ENSP00000385980.1:n.*448A>C
ENST00000407467.5:c.*448A>C	ENSP00000384691.1:n.*448A>C
NM_003394.3:c.1166A>C	NP_003385.2:p.Lys389Thr
XM_011538721.1:c.800A>C	XP_011537023.1:p.Lys267Thr
XM_011538722.1:c.800A>C	XP_011537024.1:p.Lys267Thr
XM_017019919.1:c.800A>C	XP_016875408.1:p.Lys267Thr
XM_024449179.1:c.800A>C	XP_024304947.1:p.Lys267Thr
NM_003394.4:c.1166A>C MANE Select	NP_003385.2:p.Lys389Thr