Canonical Allele Identifier: CA463242907

Gene: AGO2

Linked Data

• MyVariant Identifiers: chr8:g.141561404C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140551305C>G , CM000670.2:g.140551305C>G	GRCh38
NC_000008.10:g.141561404C>G , CM000670.1:g.141561404C>G	GRCh37
NC_000008.9:g.141630586C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000220592.10:c.1401G>C MANE Select	ENSP00000220592.5:p.Leu467=
ENST00000220592.9:c.1401G>C	ENSP00000220592.5:p.Leu467=
ENST00000519980.5:c.1401G>C	ENSP00000430176.1:p.Leu467=
ENST00000523609.5:c.*986G>C	ENSP00000430164.1:n.*986G>C
NM_001164623.1:c.1401G>C	NP_001158095.1:p.Leu467=
NM_012154.3:c.1401G>C	NP_036286.2:p.Leu467=
XM_011516964.1:c.1488G>C	XP_011515266.1:p.Leu496=
XM_011516965.1:c.1443G>C	XP_011515267.1:p.Leu481=
XM_011516966.1:c.1263G>C	XP_011515268.1:p.Leu421=
XM_011516967.1:c.1170G>C	XP_011515269.1:p.Leu390=
XM_011516968.1:c.1263G>C	XP_011515270.1:p.Leu421=
NM_001164623.2:c.1401G>C	NP_001158095.1:p.Leu467=
NM_012154.4:c.1401G>C	NP_036286.2:p.Leu467=
XM_011516965.2:c.1443G>C	XP_011515267.1:p.Leu481=
XM_011516966.3:c.1263G>C	XP_011515268.1:p.Leu421=
XM_011516968.2:c.1578G>C	XP_011515270.2:p.Leu526=
XM_017013317.2:c.1170G>C	XP_016868806.1:p.Leu390=
NM_012154.5:c.1401G>C MANE Select	NP_036286.2:p.Leu467=
NM_001164623.3:c.1401G>C	NP_001158095.1:p.Leu467=