Canonical Allele Identifier: CA350140481

Gene: ICOS

Linked Data

• ClinVar Variation Id: 1002484
• ClinVar RCV Id: RCV001298917
• dbSNP Id: rs1690083811
• MyVariant Identifiers: chr2:g.204821453T>G (hg19) ; chr2:g.203956730T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203956730T>G , CM000664.2:g.203956730T>G	GRCh38
NC_000002.11:g.204821453T>G , CM000664.1:g.204821453T>G	GRCh37
NC_000002.10:g.204529698T>G	NCBI36
NG_011586.1:g.24951T>G , LRG_65:g.24951T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316386.11:c.466T>G MANE Select	ENSP00000319476.6:p.Leu156Val
ENST00000316386.10:c.466T>G	ENSP00000319476.6:p.Leu156Val
ENST00000435193.1:c.466T>G	ENSP00000415951.1:p.Leu156Val
NM_012092.3:c.466T>G , LRG_65t1:c.466T>G	NP_036224.1:p.Leu156Val
XM_011511028.1:c.466T>G	XP_011509330.1:p.Leu156Val
XM_011511029.1:c.469T>G	XP_011509331.1:p.Leu157Val
XM_011511030.1:c.379T>G	XP_011509332.1:p.Leu127Val
XM_011511031.1:c.379T>G	XP_011509333.1:p.Leu127Val
NM_012092.4:c.466T>G MANE Select	NP_036224.1:p.Leu156Val