Canonical Allele Identifier: CA10613681
Gene: ICOS HGNC NCBI

Linked Data

ClinVar Variation Id: 333747
dbSNP Id: rs4404254

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203960563T>C , CM000664.2:g.203960563T>C GRCh38
NC_000002.11:g.204825286T>C , CM000664.1:g.204825286T>C GRCh37
NC_000002.10:g.204533531T>C NCBI36
NG_011586.1:g.28784T>C , LRG_65:g.28784T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000316386.11:c.*964T>C MANE Select ENSP00000319476.6:n.*964T>C
ENST00000316386.10:c.*964T>C ENSP00000319476.6:n.*964T>C
ENST00000435193.1:c.*972T>C ENSP00000415951.1:n.*972T>C
NM_012092.3:c.*964T>C , LRG_65t1:c.*964T>C NP_036224.1:n.*964T>C
XM_011511028.1:c.*1065T>C XP_011509330.1:n.*1065T>C
XM_011511029.1:c.*964T>C XP_011509331.1:n.*964T>C
XM_011511030.1:c.*1065T>C XP_011509332.1:n.*1065T>C
XM_011511031.1:c.*1065T>C XP_011509333.1:n.*1065T>C
NM_012092.4:c.*964T>C MANE Select NP_036224.1:n.*964T>C