Canonical Allele Identifier: CA410110002

Gene: IL10RB

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33279897G>C , CM000683.2:g.33279897G>C	GRCh38
NC_000021.8:g.34652202G>C , CM000683.1:g.34652202G>C	GRCh37
NC_000021.7:g.33574072G>C	NCBI36
NG_012089.1:g.18531G>C , LRG_152:g.18531G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000628.5:c.477G>C MANE Select	NP_000619.3:p.Trp159Cys
ENST00000290200.7:c.477G>C MANE Select	ENSP00000290200.2:p.Trp159Cys
NM_000628.4:c.477G>C	NP_000619.3:p.Trp159Cys
ENST00000290200.6:c.477G>C	ENSP00000290200.2:p.Trp159Cys
ENST00000422891.5:c.*103G>C	ENSP00000414682.1:n.*103G>C
ENST00000432231.1:c.613G>C
ENST00000433395.6:c.860G>C
ENST00000433395.7:c.1137G>C	ENSP00000388223.3:p.Trp379Cys
ENST00000451065.1:c.288G>C	ENSP00000397611.1:p.Trp96Cys
ENST00000493295.5:n.894G>C
ENST00000498371.1:n.382G>C
ENST00000609556.3:c.477G>C	ENSP00000489965.2:p.Trp159Cys
ENST00000637650.2:c.477G>C	ENSP00000489716.2:p.Trp159Cys
ENST00000646150.1:c.*565G>C	ENSP00000496248.1:n.*565G>C
ENST00000682009.1:c.*587G>C	ENSP00000506919.1:n.*587G>C
ENST00000683116.1:c.*729G>C	ENSP00000508125.1:n.*729G>C
ENST00000696764.1:n.530G>C
ENST00000696765.1:n.207+3144G>C