Canonical Allele Identifier: CA320141896

Gene: IL10RB

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33268488G>A , CM000683.2:g.33268488G>A	GRCh38
NC_000021.8:g.34640793G>A , CM000683.1:g.34640793G>A	GRCh37
NC_000021.7:g.33562663G>A	NCBI36
NG_012089.1:g.7122G>A , LRG_152:g.7122G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000628.5:c.144G>A MANE Select	NP_000619.3:p.Gly48=
ENST00000290200.7:c.144G>A MANE Select	ENSP00000290200.2:p.Gly48=
NM_000628.4:c.144G>A	NP_000619.3:p.Gly48=
ENST00000290200.6:c.144G>A	ENSP00000290200.2:p.Gly48=
ENST00000422891.5:c.144G>A	ENSP00000414682.1:p.Gly48=
ENST00000432231.1:c.310-8108G>A
ENST00000433395.6:c.527G>A
ENST00000433395.7:c.804G>A	ENSP00000388223.3:p.Gly268=
ENST00000493295.5:n.561G>A
ENST00000498371.1:n.207G>A
ENST00000609556.3:c.144G>A	ENSP00000489965.2:p.Gly48=
ENST00000637650.2:c.144G>A	ENSP00000489716.2:p.Gly48=
ENST00000646150.1:c.*232G>A	ENSP00000496248.1:n.*232G>A
ENST00000682009.1:c.*254G>A	ENSP00000506919.1:n.*254G>A
ENST00000683116.1:c.*396G>A	ENSP00000508125.1:n.*396G>A
ENST00000696764.1:n.197G>A
ENST00000696765.1:n.20G>A