Canonical Allele Identifier: CA2618595855

Gene: WNT10B

Linked Data

• gnomAD v4: 12-48965824-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48965824G>A , CM000674.2:g.48965824G>A	GRCh38
NC_000012.11:g.49359607G>A , CM000674.1:g.49359607G>A	GRCh37
NC_000012.10:g.47645874G>A	NCBI36
NG_023347.1:g.11035C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301061.9:c.*271C>T MANE Select	ENSP00000301061.4:n.*271C>T
ENST00000301061.8:c.*271C>T	ENSP00000301061.4:n.*271C>T
ENST00000403957.5:c.*723C>T	ENSP00000385980.1:n.*723C>T
ENST00000407467.5:c.*723C>T	ENSP00000384691.1:n.*723C>T
NM_003394.3:c.*271C>T	NP_003385.2:n.*271C>T
XM_011538721.1:c.*271C>T	XP_011537023.1:n.*271C>T
XM_011538722.1:c.*271C>T	XP_011537024.1:n.*271C>T
XM_017019919.1:c.*271C>T	XP_016875408.1:n.*271C>T
XM_024449179.1:c.*271C>T	XP_024304947.1:n.*271C>T
NM_003394.4:c.*271C>T MANE Select	NP_003385.2:n.*271C>T