Canonical Allele Identifier: CA2067222

Gene: ICOS

Linked Data

• ClinVar Variation Id: 282569
• ClinVar RCV Id: RCV000380646 ; RCV001088933
• dbSNP Id: rs201031378
• ExAC: 2:204820405 C / T
• gnomAD v2: 2-204820405-C-T
• gnomAD v3: 2-203955682-C-T
• gnomAD v4: 2-203955682-C-T
• MyVariant Identifiers: chr2:g.204820405C>T (hg19) ; chr2:g.203955682C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203955682C>T , CM000664.2:g.203955682C>T	GRCh38
NC_000002.11:g.204820405C>T , CM000664.1:g.204820405C>T	GRCh37
NC_000002.10:g.204528650C>T	NCBI36
NG_011586.1:g.23903C>T , LRG_65:g.23903C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316386.11:c.105C>T MANE Select	ENSP00000319476.6:p.Asn35=
ENST00000316386.10:c.105C>T	ENSP00000319476.6:p.Asn35=
ENST00000435193.1:c.105C>T	ENSP00000415951.1:p.Asn35=
NM_012092.3:c.105C>T , LRG_65t1:c.105C>T	NP_036224.1:p.Asn35=
XM_011511028.1:c.105C>T	XP_011509330.1:p.Asn35=
XM_011511029.1:c.108C>T	XP_011509331.1:p.Asn36=
XM_011511030.1:c.18C>T	XP_011509332.1:p.Asn6=
XM_011511031.1:c.18C>T	XP_011509333.1:p.Asn6=
NM_012092.4:c.105C>T MANE Select	NP_036224.1:p.Asn35=