Canonical Allele Identifier: CA772518969

Gene: WNT9B LRRC37A2

Linked Data

• dbSNP Id: rs1449322456
• MyVariant Identifiers: chr17:g.44949101A>G (hg19) ; chr17:g.46871735A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46871735A>G , CM000679.2:g.46871735A>G	GRCh38
NC_000017.10:g.44949101A>G , CM000679.1:g.44949101A>G	GRCh37
NC_000017.9:g.42304100A>G	NCBI36
NG_029164.1:g.25134A>G
NG_029164.3:g.25134A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000290015.7:c.78-782A>G (WNT9B) MANE Select	ENSP00000290015.2:n.78-782A>G
ENST00000290015.6:c.78-782A>G (WNT9B)	ENSP00000290015.2:n.78-782A>G
ENST00000393461.2:c.78-782A>G (WNT9B)	ENSP00000377105.2:n.78-782A>G
ENST00000575372.5:c.96-782A>G (WNT9B)	ENSP00000458192.1:n.96-782A>G
NM_003396.1:c.78-782A>G (WNT9B)	NP_003387.1:n.78-782A>G
XM_005257637.2:c.78-782A>G (WNT9B)	XP_005257694.1:n.78-782A>G
XM_011525178.1:c.96-782A>G (WNT9B)	XP_011523480.1:n.96-782A>G
NM_001320458.1:c.78-782A>G (WNT9B)	NP_001307387.1:n.78-782A>G
NM_003396.2:c.78-782A>G (WNT9B)	NP_003387.1:n.78-782A>G
XM_011525178.2:c.96-782A>G (WNT9B)	XP_011523480.1:n.96-782A>G
XM_024450773.1:c.4810-177321A>G (LRRC37A2)	XP_024306541.1:n.4810-177321A>G
NM_003396.3:c.78-782A>G (WNT9B) MANE Select	NP_003387.1:n.78-782A>G
NM_001320458.2:c.78-782A>G (WNT9B)	NP_001307387.1:n.78-782A>G