Canonical Allele Identifier: CA320140028

Gene: IL10RB

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33266504G>A , CM000683.2:g.33266504G>A	GRCh38
NC_000021.8:g.34638809G>A , CM000683.1:g.34638809G>A	GRCh37
NC_000021.7:g.33560679G>A	NCBI36
NG_012089.1:g.5138G>A , LRG_152:g.5138G>A
NG_016003.1:g.41579G>A
NG_016003.2:g.41579G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000628.5:c.39G>A MANE Select	NP_000619.3:p.Leu13=
ENST00000290200.7:c.39G>A MANE Select	ENSP00000290200.2:p.Leu13=
NM_000628.4:c.39G>A	NP_000619.3:p.Leu13=
ENST00000290200.6:c.39G>A	ENSP00000290200.2:p.Leu13=
ENST00000422891.5:c.39G>A	ENSP00000414682.1:p.Leu13=
ENST00000432231.1:c.310-10092G>A
ENST00000433395.6:c.433-1890G>A
ENST00000433395.7:c.710-1890G>A	ENSP00000388223.3:n.710-1890G>A
ENST00000609556.3:c.39G>A	ENSP00000489965.2:p.Leu13=
ENST00000637650.2:c.39G>A	ENSP00000489716.2:p.Leu13=
ENST00000646150.1:c.*138-1890G>A	ENSP00000496248.1:n.*138-1890G>A
ENST00000682009.1:c.*159+329G>A	ENSP00000506919.1:n.*159+329G>A
ENST00000683116.1:c.*301+329G>A	ENSP00000508125.1:n.*301+329G>A
ENST00000696764.1:n.92G>A