Canonical Allele Identifier: CA2575143608

Gene: WNT10B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48966074G>A , CM000674.2:g.48966074G>A	GRCh38
NC_000012.11:g.49359857G>A , CM000674.1:g.49359857G>A	GRCh37
NC_000012.10:g.47646124G>A	NCBI36
NG_023347.1:g.10785C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301061.9:c.*21C>T MANE Select	ENSP00000301061.4:n.*21C>T
ENST00000301061.8:c.*21C>T	ENSP00000301061.4:n.*21C>T
ENST00000403957.5:c.*473C>T	ENSP00000385980.1:n.*473C>T
ENST00000407467.5:c.*473C>T	ENSP00000384691.1:n.*473C>T
NM_003394.3:c.*21C>T	NP_003385.2:n.*21C>T
XM_011538721.1:c.*21C>T	XP_011537023.1:n.*21C>T
XM_011538722.1:c.*21C>T	XP_011537024.1:n.*21C>T
XM_017019919.1:c.*21C>T	XP_016875408.1:n.*21C>T
XM_024449179.1:c.*21C>T	XP_024304947.1:n.*21C>T
NM_003394.4:c.*21C>T MANE Select	NP_003385.2:n.*21C>T