Canonical Allele Identifier: CA384670762

Gene: WNT10B

Linked Data

• MyVariant Identifiers: chr12:g.49359892T>G (hg19) ; chr12:g.48966109T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48966109T>G , CM000674.2:g.48966109T>G	GRCh38
NC_000012.11:g.49359892T>G , CM000674.1:g.49359892T>G	GRCh37
NC_000012.10:g.47646159T>G	NCBI36
NG_023347.1:g.10750A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000301061.9:c.1156A>C MANE Select	ENSP00000301061.4:p.Asn386His
ENST00000301061.8:c.1156A>C	ENSP00000301061.4:p.Asn386His
ENST00000403957.5:c.*438A>C	ENSP00000385980.1:n.*438A>C
ENST00000407467.5:c.*438A>C	ENSP00000384691.1:n.*438A>C
NM_003394.3:c.1156A>C	NP_003385.2:p.Asn386His
XM_011538721.1:c.790A>C	XP_011537023.1:p.Asn264His
XM_011538722.1:c.790A>C	XP_011537024.1:p.Asn264His
XM_017019919.1:c.790A>C	XP_016875408.1:p.Asn264His
XM_024449179.1:c.790A>C	XP_024304947.1:p.Asn264His
NM_003394.4:c.1156A>C MANE Select	NP_003385.2:p.Asn386His