Canonical Allele Identifier: CA915953137

Gene: IL10RB

Linked Data

• ClinVar Variation Id: 756819
• ClinVar RCV Id: RCV000934348

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33268482_33268483delinsTG , CM000683.2:g.33268482_33268483delinsTG	GRCh38
NC_000021.8:g.34640787_34640788delinsTG , CM000683.1:g.34640787_34640788delinsTG	GRCh37
NC_000021.7:g.33562657_33562658delinsTG	NCBI36
NG_012089.1:g.7116_7117delinsTG , LRG_152:g.7116_7117delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433395.7:c.798_799delinsTG	ENSP00000388223.3:p.Lys267Glu
ENST00000609556.3:c.138_139delinsTG	ENSP00000489965.2:p.Lys47Glu
ENST00000637650.2:c.138_139delinsTG	ENSP00000489716.2:p.Lys47Glu
ENST00000696764.1:n.191_192delinsTG
ENST00000696765.1:n.14_15delinsTG
ENST00000682009.1:c.*248_*249delinsTG	ENSP00000506919.1:n.*248_*249delinsTG
ENST00000683116.1:c.*390_*391delinsTG	ENSP00000508125.1:n.*390_*391delinsTG
ENST00000290200.7:c.138_139delinsTG MANE Select	ENSP00000290200.2:p.Lys47Glu
ENST00000646150.1:c.*226_*227delinsTG	ENSP00000496248.1:n.*226_*227delinsTG
ENST00000290200.6:c.138_139delinsTG	ENSP00000290200.2:p.Lys47Glu
ENST00000422891.5:c.138_139delinsTG	ENSP00000414682.1:p.Lys47Glu
ENST00000432231.1:c.310-8114_310-8113delinsTG
ENST00000433395.6:c.521_522delinsTG
ENST00000493295.5:n.555_556delinsTG
ENST00000498371.1:n.201_202delinsTG
NM_000628.4:c.138_139delinsTG	NP_000619.3:p.Lys47Glu
NM_000628.5:c.138_139delinsTG MANE Select	NP_000619.3:p.Lys47Glu