Canonical Allele Identifier: CA2618595959

Gene: WNT10B

Linked Data

• gnomAD v4: 12-48965928-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48965928C>G , CM000674.2:g.48965928C>G	GRCh38
NC_000012.11:g.49359711C>G , CM000674.1:g.49359711C>G	GRCh37
NC_000012.10:g.47645978C>G	NCBI36
NG_023347.1:g.10931G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301061.9:c.*167G>C MANE Select	ENSP00000301061.4:n.*167G>C
ENST00000301061.8:c.*167G>C	ENSP00000301061.4:n.*167G>C
ENST00000403957.5:c.*619G>C	ENSP00000385980.1:n.*619G>C
ENST00000407467.5:c.*619G>C	ENSP00000384691.1:n.*619G>C
NM_003394.3:c.*167G>C	NP_003385.2:n.*167G>C
XM_011538721.1:c.*167G>C	XP_011537023.1:n.*167G>C
XM_011538722.1:c.*167G>C	XP_011537024.1:n.*167G>C
XM_017019919.1:c.*167G>C	XP_016875408.1:n.*167G>C
XM_024449179.1:c.*167G>C	XP_024304947.1:n.*167G>C
NM_003394.4:c.*167G>C MANE Select	NP_003385.2:n.*167G>C