Canonical Allele Identifier: CA236626289

Gene: WNT10B

Linked Data

• dbSNP Id: rs913946302
• gnomAD v2: 12-49359563-A-C
• gnomAD v3: 12-48965780-A-C
• gnomAD v4: 12-48965780-A-C
• MyVariant Identifiers: chr12:g.49359563A>C (hg19) ; chr12:g.48965780A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48965780A>C , CM000674.2:g.48965780A>C	GRCh38
NC_000012.11:g.49359563A>C , CM000674.1:g.49359563A>C	GRCh37
NC_000012.10:g.47645830A>C	NCBI36
NG_023347.1:g.11079T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301061.9:c.*315T>G MANE Select	ENSP00000301061.4:n.*315T>G
ENST00000301061.8:c.*315T>G	ENSP00000301061.4:n.*315T>G
ENST00000403957.5:c.*767T>G	ENSP00000385980.1:n.*767T>G
ENST00000407467.5:c.*767T>G	ENSP00000384691.1:n.*767T>G
NM_003394.3:c.*315T>G	NP_003385.2:n.*315T>G
XM_011538721.1:c.*315T>G	XP_011537023.1:n.*315T>G
XM_011538722.1:c.*315T>G	XP_011537024.1:n.*315T>G
XM_017019919.1:c.*315T>G	XP_016875408.1:n.*315T>G
XM_024449179.1:c.*315T>G	XP_024304947.1:n.*315T>G
NM_003394.4:c.*315T>G MANE Select	NP_003385.2:n.*315T>G