Canonical Allele Identifier: CA512189882

Gene: IL10RB

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33268396T>C , CM000683.2:g.33268396T>C	GRCh38
NC_000021.8:g.34640701T>C , CM000683.1:g.34640701T>C	GRCh37
NC_000021.7:g.33562571T>C	NCBI36
NG_012089.1:g.7030T>C , LRG_152:g.7030T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000628.5:c.52T>C MANE Select	NP_000619.3:p.Leu18=
ENST00000290200.7:c.52T>C MANE Select	ENSP00000290200.2:p.Leu18=
NM_000628.4:c.52T>C	NP_000619.3:p.Leu18=
ENST00000290200.6:c.52T>C	ENSP00000290200.2:p.Leu18=
ENST00000422891.5:c.52T>C	ENSP00000414682.1:p.Leu18=
ENST00000432231.1:c.310-8200T>C
ENST00000433395.6:c.435T>C
ENST00000433395.7:c.712T>C	ENSP00000388223.3:p.Leu238=
ENST00000493295.5:n.469T>C
ENST00000498371.1:n.115T>C
ENST00000609556.3:c.52T>C	ENSP00000489965.2:p.Leu18=
ENST00000637650.2:c.52T>C	ENSP00000489716.2:p.Leu18=
ENST00000646150.1:c.*140T>C	ENSP00000496248.1:n.*140T>C
ENST00000682009.1:c.*162T>C	ENSP00000506919.1:n.*162T>C
ENST00000683116.1:c.*304T>C	ENSP00000508125.1:n.*304T>C
ENST00000696764.1:n.105T>C