Canonical Allele Identifier: CA2577220183
Gene: ICOS HGNC NCBI

Linked Data

gnomAD v4: 2-203936963-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203936963C>A , CM000664.2:g.203936963C>A GRCh38
NC_000002.11:g.204801686C>A , CM000664.1:g.204801686C>A GRCh37
NC_000002.10:g.204509931C>A NCBI36
NG_011586.1:g.5184C>A , LRG_65:g.5184C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000316386.11:c.58+91C>A MANE Select ENSP00000319476.6:n.58+91C>A
ENST00000316386.10:c.58+91C>A ENSP00000319476.6:n.58+91C>A
ENST00000435193.1:c.58+91C>A ENSP00000415951.1:n.58+91C>A
NM_012092.3:c.58+91C>A , LRG_65t1:c.58+91C>A NP_036224.1:n.58+91C>A
XM_011511028.1:c.58+91C>A XP_011509330.1:n.58+91C>A
XM_011511030.1:c.-360+91C>A XP_011509332.1:n.-360+91C>A
XM_011511031.1:c.-264+91C>A XP_011509333.1:n.-264+91C>A
XR_427213.2:n.366+354G>T
XR_001739861.1:n.380+354G>T
XR_427213.3:n.380+354G>T
NM_012092.4:c.58+91C>A MANE Select NP_036224.1:n.58+91C>A
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