Canonical Allele Identifier: CA689532796

Gene: WNT10B

Linked Data

• dbSNP Id: rs1338201928
• gnomAD v3: 12-48965828-C-T
• gnomAD v4: 12-48965828-C-T
• MyVariant Identifiers: chr12:g.49359611C>T (hg19) ; chr12:g.48965828C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48965828C>T , CM000674.2:g.48965828C>T	GRCh38
NC_000012.11:g.49359611C>T , CM000674.1:g.49359611C>T	GRCh37
NC_000012.10:g.47645878C>T	NCBI36
NG_023347.1:g.11031G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301061.9:c.*267G>A MANE Select	ENSP00000301061.4:n.*267G>A
ENST00000301061.8:c.*267G>A	ENSP00000301061.4:n.*267G>A
ENST00000403957.5:c.*719G>A	ENSP00000385980.1:n.*719G>A
ENST00000407467.5:c.*719G>A	ENSP00000384691.1:n.*719G>A
NM_003394.3:c.*267G>A	NP_003385.2:n.*267G>A
XM_011538721.1:c.*267G>A	XP_011537023.1:n.*267G>A
XM_011538722.1:c.*267G>A	XP_011537024.1:n.*267G>A
XM_017019919.1:c.*267G>A	XP_016875408.1:n.*267G>A
XM_024449179.1:c.*267G>A	XP_024304947.1:n.*267G>A
NM_003394.4:c.*267G>A MANE Select	NP_003385.2:n.*267G>A