Canonical Allele Identifier: CA2618595890

Gene: WNT10B

Linked Data

• gnomAD v4: 12-48965861-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48965861T>G , CM000674.2:g.48965861T>G	GRCh38
NC_000012.11:g.49359644T>G , CM000674.1:g.49359644T>G	GRCh37
NC_000012.10:g.47645911T>G	NCBI36
NG_023347.1:g.10998A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301061.9:c.*234A>C MANE Select	ENSP00000301061.4:n.*234A>C
ENST00000301061.8:c.*234A>C	ENSP00000301061.4:n.*234A>C
ENST00000403957.5:c.*686A>C	ENSP00000385980.1:n.*686A>C
ENST00000407467.5:c.*686A>C	ENSP00000384691.1:n.*686A>C
NM_003394.3:c.*234A>C	NP_003385.2:n.*234A>C
XM_011538721.1:c.*234A>C	XP_011537023.1:n.*234A>C
XM_011538722.1:c.*234A>C	XP_011537024.1:n.*234A>C
XM_017019919.1:c.*234A>C	XP_016875408.1:n.*234A>C
XM_024449179.1:c.*234A>C	XP_024304947.1:n.*234A>C
NM_003394.4:c.*234A>C MANE Select	NP_003385.2:n.*234A>C