Canonical Allele Identifier: CA585314664

Gene: AGO2

Linked Data

• dbSNP Id: rs746526626
• gnomAD v2: 8-141561397-C-G
• gnomAD v4: 8-140551298-C-G
• MyVariant Identifiers: chr8:g.141561397C>G (hg19) ; chr8:g.140551298C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140551298C>G , CM000670.2:g.140551298C>G	GRCh38
NC_000008.10:g.141561397C>G , CM000670.1:g.141561397C>G	GRCh37
NC_000008.9:g.141630579C>G	NCBI36

Transcript Alleles

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