Canonical Allele Identifier: CA763556370

Gene: ICOS

Linked Data

• dbSNP Id: rs10932029
• MyVariant Identifiers: chr2:g.204801768T>A (hg19) ; chr2:g.203937045T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203937045T>A , CM000664.2:g.203937045T>A	GRCh38
NC_000002.11:g.204801768T>A , CM000664.1:g.204801768T>A	GRCh37
NC_000002.10:g.204510013T>A	NCBI36
NG_011586.1:g.5266T>A , LRG_65:g.5266T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000316386.11:c.58+173T>A MANE Select	ENSP00000319476.6:n.58+173T>A
ENST00000316386.10:c.58+173T>A	ENSP00000319476.6:n.58+173T>A
ENST00000435193.1:c.58+173T>A	ENSP00000415951.1:n.58+173T>A
NM_012092.3:c.58+173T>A , LRG_65t1:c.58+173T>A	NP_036224.1:n.58+173T>A
XM_011511028.1:c.58+173T>A	XP_011509330.1:n.58+173T>A
XM_011511030.1:c.-360+173T>A	XP_011509332.1:n.-360+173T>A
XM_011511031.1:c.-264+173T>A	XP_011509333.1:n.-264+173T>A
XR_427213.2:n.366+272A>T
XR_001739861.1:n.380+272A>T
XR_427213.3:n.380+272A>T
NM_012092.4:c.58+173T>A MANE Select	NP_036224.1:n.58+173T>A