Canonical Allele Identifier: CA10006130

Gene: IL10RB

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33279803A>T , CM000683.2:g.33279803A>T	GRCh38
NC_000021.8:g.34652108A>T , CM000683.1:g.34652108A>T	GRCh37
NC_000021.7:g.33573978A>T	NCBI36
NG_012089.1:g.18437A>T , LRG_152:g.18437A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000628.5:c.383A>T MANE Select	NP_000619.3:p.His128Leu
ENST00000290200.7:c.383A>T MANE Select	ENSP00000290200.2:p.His128Leu
NM_000628.4:c.383A>T	NP_000619.3:p.His128Leu
ENST00000290200.6:c.383A>T	ENSP00000290200.2:p.His128Leu
ENST00000422891.5:c.*9A>T	ENSP00000414682.1:n.*9A>T
ENST00000432231.1:c.519A>T
ENST00000433395.6:c.766A>T
ENST00000433395.7:c.1043A>T	ENSP00000388223.3:p.His348Leu
ENST00000451065.1:c.194A>T	ENSP00000397611.1:p.His65Leu
ENST00000493295.5:n.800A>T
ENST00000498371.1:n.288A>T
ENST00000609556.3:c.383A>T	ENSP00000489965.2:p.His128Leu
ENST00000637650.2:c.383A>T	ENSP00000489716.2:p.His128Leu
ENST00000646150.1:c.*471A>T	ENSP00000496248.1:n.*471A>T
ENST00000682009.1:c.*493A>T	ENSP00000506919.1:n.*493A>T
ENST00000683116.1:c.*635A>T	ENSP00000508125.1:n.*635A>T
ENST00000696764.1:n.436A>T
ENST00000696765.1:n.207+3050A>T