Canonical Allele Identifier: CA2618595995

Gene: WNT10B

Linked Data

• gnomAD v4: 12-48965959-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48965959C>A , CM000674.2:g.48965959C>A	GRCh38
NC_000012.11:g.49359742C>A , CM000674.1:g.49359742C>A	GRCh37
NC_000012.10:g.47646009C>A	NCBI36
NG_023347.1:g.10900G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301061.9:c.*136G>T MANE Select	ENSP00000301061.4:n.*136G>T
ENST00000301061.8:c.*136G>T	ENSP00000301061.4:n.*136G>T
ENST00000403957.5:c.*588G>T	ENSP00000385980.1:n.*588G>T
ENST00000407467.5:c.*588G>T	ENSP00000384691.1:n.*588G>T
NM_003394.3:c.*136G>T	NP_003385.2:n.*136G>T
XM_011538721.1:c.*136G>T	XP_011537023.1:n.*136G>T
XM_011538722.1:c.*136G>T	XP_011537024.1:n.*136G>T
XM_017019919.1:c.*136G>T	XP_016875408.1:n.*136G>T
XM_024449179.1:c.*136G>T	XP_024304947.1:n.*136G>T
NM_003394.4:c.*136G>T MANE Select	NP_003385.2:n.*136G>T