Canonical Allele Identifier: CA689532859

Gene: WNT10B

Linked Data

• dbSNP Id: rs1263066392
• gnomAD v4: 12-48965996-A-G
• MyVariant Identifiers: chr12:g.49359779A>G (hg19) ; chr12:g.48965996A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48965996A>G , CM000674.2:g.48965996A>G	GRCh38
NC_000012.11:g.49359779A>G , CM000674.1:g.49359779A>G	GRCh37
NC_000012.10:g.47646046A>G	NCBI36
NG_023347.1:g.10863T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301061.9:c.*99T>C MANE Select	ENSP00000301061.4:n.*99T>C
ENST00000301061.8:c.*99T>C	ENSP00000301061.4:n.*99T>C
ENST00000403957.5:c.*551T>C	ENSP00000385980.1:n.*551T>C
ENST00000407467.5:c.*551T>C	ENSP00000384691.1:n.*551T>C
NM_003394.3:c.*99T>C	NP_003385.2:n.*99T>C
XM_011538721.1:c.*99T>C	XP_011537023.1:n.*99T>C
XM_011538722.1:c.*99T>C	XP_011537024.1:n.*99T>C
XM_017019919.1:c.*99T>C	XP_016875408.1:n.*99T>C
XM_024449179.1:c.*99T>C	XP_024304947.1:n.*99T>C
NM_003394.4:c.*99T>C MANE Select	NP_003385.2:n.*99T>C