Canonical Allele Identifier: CA2662769788
Gene: ICOS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203936961G>A , CM000664.2:g.203936961G>A GRCh38
NC_000002.11:g.204801684G>A , CM000664.1:g.204801684G>A GRCh37
NC_000002.10:g.204509929G>A NCBI36
NG_011586.1:g.5182G>A , LRG_65:g.5182G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000316386.11:c.58+89G>A MANE Select ENSP00000319476.6:n.58+89G>A
ENST00000316386.10:c.58+89G>A ENSP00000319476.6:n.58+89G>A
ENST00000435193.1:c.58+89G>A ENSP00000415951.1:n.58+89G>A
NM_012092.3:c.58+89G>A , LRG_65t1:c.58+89G>A NP_036224.1:n.58+89G>A
XM_011511028.1:c.58+89G>A XP_011509330.1:n.58+89G>A
XM_011511030.1:c.-360+89G>A XP_011509332.1:n.-360+89G>A
XM_011511031.1:c.-264+89G>A XP_011509333.1:n.-264+89G>A
XR_427213.2:n.366+356C>T
XR_001739861.1:n.380+356C>T
XR_427213.3:n.380+356C>T
NM_012092.4:c.58+89G>A MANE Select NP_036224.1:n.58+89G>A