Canonical Allele Identifier: CA12919358

Gene: AGO2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140564095A>G , CM000670.2:g.140564095A>G	GRCh38
NC_000008.10:g.141574194A>G , CM000670.1:g.141574194A>G	GRCh37
NC_000008.9:g.141643376A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220592.10:c.337-1461T>C MANE Select	ENSP00000220592.5:n.337-1461T>C
ENST00000220592.9:c.337-1461T>C	ENSP00000220592.5:n.337-1461T>C
ENST00000519980.5:c.337-1461T>C	ENSP00000430176.1:n.337-1461T>C
ENST00000523609.5:c.144-1461T>C	ENSP00000430164.1:n.144-1461T>C
NM_001164623.1:c.337-1461T>C	NP_001158095.1:n.337-1461T>C
NM_012154.3:c.337-1461T>C	NP_036286.2:n.337-1461T>C
XM_011516964.1:c.424-1461T>C	XP_011515266.1:n.424-1461T>C
XM_011516965.1:c.379-1461T>C	XP_011515267.1:n.379-1461T>C
XM_011516966.1:c.199-1461T>C	XP_011515268.1:n.199-1461T>C
XM_011516967.1:c.106-1461T>C	XP_011515269.1:n.106-1461T>C
XM_011516968.1:c.199-1461T>C	XP_011515270.1:n.199-1461T>C
NM_001164623.2:c.337-1461T>C	NP_001158095.1:n.337-1461T>C
NM_012154.4:c.337-1461T>C	NP_036286.2:n.337-1461T>C
XM_011516965.2:c.379-1461T>C	XP_011515267.1:n.379-1461T>C
XM_011516966.3:c.199-1461T>C	XP_011515268.1:n.199-1461T>C
XM_011516968.2:c.514-1461T>C	XP_011515270.2:n.514-1461T>C
XM_017013317.2:c.106-1461T>C	XP_016868806.1:n.106-1461T>C
NM_012154.5:c.337-1461T>C MANE Select	NP_036286.2:n.337-1461T>C
NM_001164623.3:c.337-1461T>C	NP_001158095.1:n.337-1461T>C