Canonical Allele Identifier: CA6544101

Gene: WNT10B

Linked Data

• ClinVar Variation Id: 253058
• ClinVar RCV Id: RCV000239472
• dbSNP Id: rs766021478
• ExAC: 12:49360262 C / T
• gnomAD v2: 12-49360262-C-T
• gnomAD v4: 12-48966479-C-T
• MyVariant Identifiers: chr12:g.49360262C>T (hg19) ; chr12:g.48966479C>T (hg38)
• PubMed: PMID:27321946

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48966479C>T , CM000674.2:g.48966479C>T	GRCh38
NC_000012.11:g.49360262C>T , CM000674.1:g.49360262C>T	GRCh37
NC_000012.10:g.47646529C>T	NCBI36
NG_023347.1:g.10380G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000301061.9:c.786G>A MANE Select	ENSP00000301061.4:p.Trp262Ter
ENST00000301061.8:c.786G>A	ENSP00000301061.4:p.Trp262Ter
ENST00000403957.5:c.*68G>A	ENSP00000385980.1:n.*68G>A
ENST00000407467.5:c.*68G>A	ENSP00000384691.1:n.*68G>A
NM_003394.3:c.786G>A	NP_003385.2:p.Trp262Ter
XM_011538721.1:c.420G>A	XP_011537023.1:p.Trp140Ter
XM_011538722.1:c.420G>A	XP_011537024.1:p.Trp140Ter
XM_011538723.1:c.*68G>A	XP_011537025.1:n.*68G>A
XM_011538724.1:c.*64G>A	XP_011537026.1:n.*64G>A
XM_017019919.1:c.420G>A	XP_016875408.1:p.Trp140Ter
XM_024449179.1:c.420G>A	XP_024304947.1:p.Trp140Ter
NM_003394.4:c.786G>A MANE Select	NP_003385.2:p.Trp262Ter