Canonical Allele Identifier: CA433554462

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064403G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026970G>C , CM000665.2:g.49026970G>C	GRCh38
NC_000003.11:g.49064403G>C , CM000665.1:g.49064403G>C	GRCh37
NC_000003.10:g.49039407G>C	NCBI36
NG_012091.1:g.7473C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2649C>G	ENSP00000515567.1:p.Arg883=
ENST00000703937.1:c.*1710C>G	ENSP00000515568.1:n.*1710C>G
ENST00000326739.9:c.609C>G MANE Select	ENSP00000321584.4:p.Arg203=
ENST00000429182.6:c.609C>G	ENSP00000393525.2:p.Arg203=
ENST00000442157.2:c.534C>G	ENSP00000403502.2:p.Arg178=
ENST00000462980.2:n.1124C>G
ENST00000472328.2:n.675C>G
ENST00000491610.2:n.496C>G
ENST00000676607.1:n.905C>G
ENST00000676627.1:n.1339C>G
ENST00000676708.1:n.1816C>G
ENST00000676864.1:n.1685C>G
ENST00000677010.1:c.645C>G	ENSP00000503089.1:p.Arg215=
ENST00000677108.1:n.2442C>G
ENST00000677168.1:n.1081C>G
ENST00000677185.1:n.1099C>G
ENST00000677205.1:n.1320C>G
ENST00000677344.1:n.1810C>G
ENST00000677480.1:c.*286C>G	ENSP00000504378.1:n.*286C>G
ENST00000677519.1:n.1319C>G
ENST00000677593.1:n.1092C>G
ENST00000677740.1:n.2041C>G
ENST00000677991.1:n.1782C>G
ENST00000678001.1:n.1102C>G
ENST00000678085.1:n.1092C>G
ENST00000678177.1:n.2385C>G
ENST00000678603.1:n.1687C>G
ENST00000678724.1:c.534C>G	ENSP00000503874.1:p.Arg178=
ENST00000678920.1:n.767C>G
ENST00000679019.1:n.1306C>G
ENST00000679117.1:c.*424C>G	ENSP00000503240.1:n.*424C>G
ENST00000679339.1:n.1377C>G
ENST00000326739.8:c.609C>G	ENSP00000321584.4:p.Arg203=
ENST00000429182.5:c.403C>G
ENST00000442157.1:c.534C>G	ENSP00000403502.1:p.Arg178=
ENST00000462980.1:n.511C>G
ENST00000491610.1:n.496C>G
NM_000884.2:c.609C>G	NP_000875.2:p.Arg203=
XM_006713128.2:c.819C>G	XP_006713191.1:p.Arg273=
XM_006713128.3:c.819C>G	XP_006713191.1:p.Arg273=
XM_017006349.1:c.744C>G	XP_016861838.1:p.Arg248=
XM_017006350.1:c.744C>G	XP_016861839.1:p.Arg248=
NM_000884.3:c.609C>G MANE Select	NP_000875.2:p.Arg203=