Canonical Allele Identifier: CA2386609602

Gene: IL10RB

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33296442A>T , CM000683.2:g.33296442A>T	GRCh38
NC_000021.8:g.34668747A>T , CM000683.1:g.34668747A>T	GRCh37
NC_000021.7:g.33590617A>T	NCBI36
NG_012089.1:g.35076A>T , LRG_152:g.35076A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433395.7:c.*85A>T	ENSP00000388223.3:n.*85A>T
ENST00000609556.3:c.804+8181A>T	ENSP00000489965.2:n.804+8181A>T
ENST00000637650.2:c.804+8181A>T	ENSP00000489716.2:n.804+8181A>T
ENST00000682009.1:c.*1173A>T	ENSP00000506919.1:n.*1173A>T
ENST00000683116.1:c.*1315A>T	ENSP00000508125.1:n.*1315A>T
ENST00000290200.7:c.*85A>T MANE Select	ENSP00000290200.2:n.*85A>T
ENST00000609556.2:c.129+8181A>T	ENSP00000489965.1:n.129+8181A>T
ENST00000637650.1:c.129+8181A>T	ENSP00000489716.1:n.129+8181A>T
ENST00000646150.1:c.*1151A>T	ENSP00000496248.1:n.*1151A>T
ENST00000290200.6:c.*85A>T	ENSP00000290200.2:n.*85A>T
ENST00000493295.5:n.1480A>T
NM_000628.4:c.*85A>T	NP_000619.3:n.*85A>T
NM_000628.5:c.*85A>T MANE Select	NP_000619.3:n.*85A>T