Canonical Allele Identifier: CA410096147

Gene: IL10RB

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33296202C>T , CM000683.2:g.33296202C>T	GRCh38
NC_000021.8:g.34668507C>T , CM000683.1:g.34668507C>T	GRCh37
NC_000021.7:g.33590377C>T	NCBI36
NG_012089.1:g.34836C>T , LRG_152:g.34836C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000628.5:c.823C>T MANE Select	NP_000619.3:p.His275Tyr
ENST00000290200.7:c.823C>T MANE Select	ENSP00000290200.2:p.His275Tyr
NM_000628.4:c.823C>T	NP_000619.3:p.His275Tyr
ENST00000290200.6:c.823C>T	ENSP00000290200.2:p.His275Tyr
ENST00000422891.5:c.*449C>T	ENSP00000414682.1:n.*449C>T
ENST00000433395.7:c.1483C>T	ENSP00000388223.3:p.His495Tyr
ENST00000451065.1:c.750C>T	ENSP00000397611.1:n.750C>T
ENST00000493295.5:n.1240C>T
ENST00000609556.2:c.129+7941C>T	ENSP00000489965.1:n.129+7941C>T
ENST00000609556.3:c.804+7941C>T	ENSP00000489965.2:n.804+7941C>T
ENST00000637650.1:c.129+7941C>T	ENSP00000489716.1:n.129+7941C>T
ENST00000637650.2:c.804+7941C>T	ENSP00000489716.2:n.804+7941C>T
ENST00000646150.1:c.*911C>T	ENSP00000496248.1:n.*911C>T
ENST00000682009.1:c.*933C>T	ENSP00000506919.1:n.*933C>T
ENST00000683116.1:c.*1075C>T	ENSP00000508125.1:n.*1075C>T