Canonical Allele Identifier: CA410107327

Gene: IL10RB

Linked Data

• dbSNP Id: rs2834167
• MyVariant Identifiers: chr21:g.34640788A>T (hg19) ; chr21:g.33268483A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33268483A>T , CM000683.2:g.33268483A>T	GRCh38
NC_000021.8:g.34640788A>T , CM000683.1:g.34640788A>T	GRCh37
NC_000021.7:g.33562658A>T	NCBI36
NG_012089.1:g.7117A>T , LRG_152:g.7117A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000433395.7:c.799A>T	ENSP00000388223.3:p.Lys267Ter
ENST00000609556.3:c.139A>T	ENSP00000489965.2:p.Lys47Ter
ENST00000637650.2:c.139A>T	ENSP00000489716.2:p.Lys47Ter
ENST00000696764.1:n.192A>T
ENST00000696765.1:n.15A>T
ENST00000682009.1:c.*249A>T	ENSP00000506919.1:n.*249A>T
ENST00000683116.1:c.*391A>T	ENSP00000508125.1:n.*391A>T
ENST00000290200.7:c.139A>T MANE Select	ENSP00000290200.2:p.Lys47Ter
ENST00000646150.1:c.*227A>T	ENSP00000496248.1:n.*227A>T
ENST00000290200.6:c.139A>T	ENSP00000290200.2:p.Lys47Ter
ENST00000422891.5:c.139A>T	ENSP00000414682.1:p.Lys47Ter
ENST00000432231.1:c.310-8113A>T
ENST00000433395.6:c.522A>T
ENST00000493295.5:n.556A>T
ENST00000498371.1:n.202A>T
NM_000628.4:c.139A>T	NP_000619.3:p.Lys47Ter
NM_000628.5:c.139A>T MANE Select	NP_000619.3:p.Lys47Ter