Canonical Allele Identifier: CA2662769783

Gene: ICOS

Linked Data

• gnomAD v4: 2-203936957-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203936957A>G , CM000664.2:g.203936957A>G	GRCh38
NC_000002.11:g.204801680A>G , CM000664.1:g.204801680A>G	GRCh37
NC_000002.10:g.204509925A>G	NCBI36
NG_011586.1:g.5178A>G , LRG_65:g.5178A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316386.11:c.58+85A>G MANE Select	ENSP00000319476.6:n.58+85A>G
ENST00000316386.10:c.58+85A>G	ENSP00000319476.6:n.58+85A>G
ENST00000435193.1:c.58+85A>G	ENSP00000415951.1:n.58+85A>G
NM_012092.3:c.58+85A>G , LRG_65t1:c.58+85A>G	NP_036224.1:n.58+85A>G
XM_011511028.1:c.58+85A>G	XP_011509330.1:n.58+85A>G
XM_011511030.1:c.-360+85A>G	XP_011509332.1:n.-360+85A>G
XM_011511031.1:c.-264+85A>G	XP_011509333.1:n.-264+85A>G
XR_427213.2:n.366+360T>C
XR_001739861.1:n.380+360T>C
XR_427213.3:n.380+360T>C
NM_012092.4:c.58+85A>G MANE Select	NP_036224.1:n.58+85A>G