Canonical Allele Identifier: CA4894433

Gene: AGO2

Linked Data

• dbSNP Id: rs2292779
• ExAC: 8:141561393 G / T
• gnomAD v2: 8-141561393-G-T
• gnomAD v3: 8-140551294-G-T
• gnomAD v4: 8-140551294-G-T
• MyVariant Identifiers: chr8:g.141561393G>T (hg19) ; chr8:g.140551294G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140551294G>T , CM000670.2:g.140551294G>T	GRCh38
NC_000008.10:g.141561393G>T , CM000670.1:g.141561393G>T	GRCh37
NC_000008.9:g.141630575G>T	NCBI36

Transcript Alleles

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