Canonical Allele Identifier: CA10652875

Gene: IL10RB

Linked Data

• ClinVar Variation Id: 339702
• ClinVar RCV Id: RCV000322001
• dbSNP Id: rs886057005
• gnomAD v2: 21-34669027-C-T
• gnomAD v3: 21-33296722-C-T
• gnomAD v4: 21-33296722-C-T
• MyVariant Identifiers: chr21:g.34669027C>T (hg19) ; chr21:g.33296722C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33296722C>T , CM000683.2:g.33296722C>T	GRCh38
NC_000021.8:g.34669027C>T , CM000683.1:g.34669027C>T	GRCh37
NC_000021.7:g.33590897C>T	NCBI36
NG_012089.1:g.35356C>T , LRG_152:g.35356C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609556.3:c.804+8461C>T	ENSP00000489965.2:n.804+8461C>T
ENST00000637650.2:c.804+8461C>T	ENSP00000489716.2:n.804+8461C>T
ENST00000682009.1:c.*1453C>T	ENSP00000506919.1:n.*1453C>T
ENST00000683116.1:c.*1595C>T	ENSP00000508125.1:n.*1595C>T
ENST00000290200.7:c.*365C>T MANE Select	ENSP00000290200.2:n.*365C>T
ENST00000609556.2:c.129+8461C>T	ENSP00000489965.1:n.129+8461C>T
ENST00000637650.1:c.129+8461C>T	ENSP00000489716.1:n.129+8461C>T
ENST00000646150.1:c.*1431C>T	ENSP00000496248.1:n.*1431C>T
ENST00000290200.6:c.*365C>T	ENSP00000290200.2:n.*365C>T
ENST00000493295.5:n.1760C>T
NM_000628.4:c.*365C>T	NP_000619.3:n.*365C>T
NM_000628.5:c.*365C>T MANE Select	NP_000619.3:n.*365C>T