Canonical Allele Identifier: CA10006210

Gene: IL10RB

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33288108G>A , CM000683.2:g.33288108G>A	GRCh38
NC_000021.8:g.34660413G>A , CM000683.1:g.34660413G>A	GRCh37
NC_000021.7:g.33582283G>A	NCBI36
NG_012089.1:g.26742G>A , LRG_152:g.26742G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000628.5:c.651G>A MANE Select	NP_000619.3:p.Thr217=
ENST00000290200.7:c.651G>A MANE Select	ENSP00000290200.2:p.Thr217=
NM_000628.4:c.651G>A	NP_000619.3:p.Thr217=
ENST00000290200.6:c.651G>A	ENSP00000290200.2:p.Thr217=
ENST00000422891.5:c.*277G>A	ENSP00000414682.1:n.*277G>A
ENST00000433395.7:c.1311G>A	ENSP00000388223.3:p.Thr437=
ENST00000451065.1:c.462G>A	ENSP00000397611.1:p.Thr154=
ENST00000493295.5:n.1068G>A
ENST00000498371.1:n.556G>A
ENST00000609556.3:c.651G>A	ENSP00000489965.2:p.Thr217=
ENST00000637650.2:c.651G>A	ENSP00000489716.2:p.Thr217=
ENST00000646150.1:c.*739G>A	ENSP00000496248.1:n.*739G>A
ENST00000682009.1:c.*761G>A	ENSP00000506919.1:n.*761G>A
ENST00000683116.1:c.*903G>A	ENSP00000508125.1:n.*903G>A
ENST00000696764.1:n.704G>A