Canonical Allele Identifier: CA1824690486
Gene: AGO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.140551196C= , CM000670.2:g.140551196C= GRCh38
NC_000008.10:g.141561295C= , CM000670.1:g.141561295C= GRCh37
NC_000008.9:g.141630477C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000220592.10:c.1403+107G= MANE Select ENSP00000220592.5:n.1403+107G=
ENST00000220592.9:c.1403+107G= ENSP00000220592.5:n.1403+107G=
ENST00000519980.5:c.1403+107G= ENSP00000430176.1:n.1403+107G=
ENST00000523609.5:c.*988+107G= ENSP00000430164.1:n.*988+107G=
NM_001164623.1:c.1403+107G= NP_001158095.1:n.1403+107G=
NM_012154.3:c.1403+107G= NP_036286.2:n.1403+107G=
XM_011516964.1:c.1490+107G= XP_011515266.1:n.1490+107G=
XM_011516965.1:c.1445+107G= XP_011515267.1:n.1445+107G=
XM_011516966.1:c.1265+107G= XP_011515268.1:n.1265+107G=
XM_011516967.1:c.1172+107G= XP_011515269.1:n.1172+107G=
XM_011516968.1:c.1265+107G= XP_011515270.1:n.1265+107G=
NM_001164623.2:c.1403+107G= NP_001158095.1:n.1403+107G=
NM_012154.4:c.1403+107G= NP_036286.2:n.1403+107G=
XM_011516965.2:c.1445+107G= XP_011515267.1:n.1445+107G=
XM_011516966.3:c.1265+107G= XP_011515268.1:n.1265+107G=
XM_011516968.2:c.1580+107G= XP_011515270.2:n.1580+107G=
XM_017013317.2:c.1172+107G= XP_016868806.1:n.1172+107G=
NM_012154.5:c.1403+107G= MANE Select NP_036286.2:n.1403+107G=
NM_001164623.3:c.1403+107G= NP_001158095.1:n.1403+107G=