Canonical Allele Identifier: CA10006165

Gene: IL10RB

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33283163C>G , CM000683.2:g.33283163C>G	GRCh38
NC_000021.8:g.34655468C>G , CM000683.1:g.34655468C>G	GRCh37
NC_000021.7:g.33577338C>G	NCBI36
NG_012089.1:g.21797C>G , LRG_152:g.21797C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000628.5:c.568C>G MANE Select	NP_000619.3:p.Gln190Glu
ENST00000290200.7:c.568C>G MANE Select	ENSP00000290200.2:p.Gln190Glu
NM_000628.4:c.568C>G	NP_000619.3:p.Gln190Glu
ENST00000290200.6:c.568C>G	ENSP00000290200.2:p.Gln190Glu
ENST00000422891.5:c.*194C>G	ENSP00000414682.1:n.*194C>G
ENST00000432231.1:c.704C>G
ENST00000433395.6:c.951C>G
ENST00000433395.7:c.1228C>G	ENSP00000388223.3:p.Gln410Glu
ENST00000451065.1:c.379C>G	ENSP00000397611.1:p.Gln127Glu
ENST00000493295.5:n.985C>G
ENST00000498371.1:n.473C>G
ENST00000609556.3:c.568C>G	ENSP00000489965.2:p.Gln190Glu
ENST00000637650.2:c.568C>G	ENSP00000489716.2:p.Gln190Glu
ENST00000646150.1:c.*656C>G	ENSP00000496248.1:n.*656C>G
ENST00000682009.1:c.*678C>G	ENSP00000506919.1:n.*678C>G
ENST00000683116.1:c.*820C>G	ENSP00000508125.1:n.*820C>G
ENST00000696764.1:n.621C>G
ENST00000696765.1:n.277C>G