Canonical Allele Identifier: CA512190301

Gene: IL10RB

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33279864G>A , CM000683.2:g.33279864G>A	GRCh38
NC_000021.8:g.34652169G>A , CM000683.1:g.34652169G>A	GRCh37
NC_000021.7:g.33574039G>A	NCBI36
NG_012089.1:g.18498G>A , LRG_152:g.18498G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000628.5:c.444G>A MANE Select	NP_000619.3:p.Val148=
ENST00000290200.7:c.444G>A MANE Select	ENSP00000290200.2:p.Val148=
NM_000628.4:c.444G>A	NP_000619.3:p.Val148=
ENST00000290200.6:c.444G>A	ENSP00000290200.2:p.Val148=
ENST00000422891.5:c.*70G>A	ENSP00000414682.1:n.*70G>A
ENST00000432231.1:c.580G>A
ENST00000433395.6:c.827G>A
ENST00000433395.7:c.1104G>A	ENSP00000388223.3:p.Val368=
ENST00000451065.1:c.255G>A	ENSP00000397611.1:p.Val85=
ENST00000493295.5:n.861G>A
ENST00000498371.1:n.349G>A
ENST00000609556.3:c.444G>A	ENSP00000489965.2:p.Val148=
ENST00000637650.2:c.444G>A	ENSP00000489716.2:p.Val148=
ENST00000646150.1:c.*532G>A	ENSP00000496248.1:n.*532G>A
ENST00000682009.1:c.*554G>A	ENSP00000506919.1:n.*554G>A
ENST00000683116.1:c.*696G>A	ENSP00000508125.1:n.*696G>A
ENST00000696764.1:n.497G>A
ENST00000696765.1:n.207+3111G>A