Canonical Allele Identifier: CA384671578

Gene: WNT10B

Linked Data

• MyVariant Identifiers: chr12:g.49359996C>A (hg19) ; chr12:g.48966213C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48966213C>A , CM000674.2:g.48966213C>A	GRCh38
NC_000012.11:g.49359996C>A , CM000674.1:g.49359996C>A	GRCh37
NC_000012.10:g.47646263C>A	NCBI36
NG_023347.1:g.10646G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301061.9:c.1052G>T MANE Select	ENSP00000301061.4:p.Arg351Leu
ENST00000301061.8:c.1052G>T	ENSP00000301061.4:p.Arg351Leu
ENST00000403957.5:c.*334G>T	ENSP00000385980.1:n.*334G>T
ENST00000407467.5:c.*334G>T	ENSP00000384691.1:n.*334G>T
NM_003394.3:c.1052G>T	NP_003385.2:p.Arg351Leu
XM_011538721.1:c.686G>T	XP_011537023.1:p.Arg229Leu
XM_011538722.1:c.686G>T	XP_011537024.1:p.Arg229Leu
XM_011538724.1:c.*330G>T	XP_011537026.1:n.*330G>T
XM_017019919.1:c.686G>T	XP_016875408.1:p.Arg229Leu
XM_024449179.1:c.686G>T	XP_024304947.1:p.Arg229Leu
NM_003394.4:c.1052G>T MANE Select	NP_003385.2:p.Arg351Leu