Canonical Allele Identifier: CA626359850

Gene: WNT9B LRRC37A2

Linked Data

• dbSNP Id: rs1195461755
• gnomAD v2: 17-44949141-T-C
• gnomAD v3: 17-46871775-T-C
• gnomAD v4: 17-46871775-T-C
• MyVariant Identifiers: chr17:g.44949141T>C (hg19) ; chr17:g.46871775T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46871775T>C , CM000679.2:g.46871775T>C	GRCh38
NC_000017.10:g.44949141T>C , CM000679.1:g.44949141T>C	GRCh37
NC_000017.9:g.42304140T>C	NCBI36
NG_029164.1:g.25174T>C
NG_029164.3:g.25174T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000290015.7:c.78-742T>C (WNT9B) MANE Select	ENSP00000290015.2:n.78-742T>C
ENST00000290015.6:c.78-742T>C (WNT9B)	ENSP00000290015.2:n.78-742T>C
ENST00000393461.2:c.78-742T>C (WNT9B)	ENSP00000377105.2:n.78-742T>C
ENST00000575372.5:c.96-742T>C (WNT9B)	ENSP00000458192.1:n.96-742T>C
NM_003396.1:c.78-742T>C (WNT9B)	NP_003387.1:n.78-742T>C
XM_005257637.2:c.78-742T>C (WNT9B)	XP_005257694.1:n.78-742T>C
XM_011525178.1:c.96-742T>C (WNT9B)	XP_011523480.1:n.96-742T>C
NM_001320458.1:c.78-742T>C (WNT9B)	NP_001307387.1:n.78-742T>C
NM_003396.2:c.78-742T>C (WNT9B)	NP_003387.1:n.78-742T>C
XM_011525178.2:c.96-742T>C (WNT9B)	XP_011523480.1:n.96-742T>C
XM_024450773.1:c.4810-177281T>C (LRRC37A2)	XP_024306541.1:n.4810-177281T>C
NM_003396.3:c.78-742T>C (WNT9B) MANE Select	NP_003387.1:n.78-742T>C
NM_001320458.2:c.78-742T>C (WNT9B)	NP_001307387.1:n.78-742T>C