Canonical Allele Identifier: CA2577220178

Gene: ICOS

Linked Data

• gnomAD v4: 2-203936950-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203936950C>A , CM000664.2:g.203936950C>A	GRCh38
NC_000002.11:g.204801673C>A , CM000664.1:g.204801673C>A	GRCh37
NC_000002.10:g.204509918C>A	NCBI36
NG_011586.1:g.5171C>A , LRG_65:g.5171C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316386.11:c.58+78C>A MANE Select	ENSP00000319476.6:n.58+78C>A
ENST00000316386.10:c.58+78C>A	ENSP00000319476.6:n.58+78C>A
ENST00000435193.1:c.58+78C>A	ENSP00000415951.1:n.58+78C>A
NM_012092.3:c.58+78C>A , LRG_65t1:c.58+78C>A	NP_036224.1:n.58+78C>A
XM_011511028.1:c.58+78C>A	XP_011509330.1:n.58+78C>A
XM_011511030.1:c.-360+78C>A	XP_011509332.1:n.-360+78C>A
XM_011511031.1:c.-264+78C>A	XP_011509333.1:n.-264+78C>A
XR_427213.2:n.366+367G>T
XR_001739861.1:n.380+367G>T
XR_427213.3:n.380+367G>T
NM_012092.4:c.58+78C>A MANE Select	NP_036224.1:n.58+78C>A