Canonical Allele Identifier: CA433629713

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064306A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026873A>T , CM000665.2:g.49026873A>T	GRCh38
NC_000003.11:g.49064306A>T , CM000665.1:g.49064306A>T	GRCh37
NC_000003.10:g.49039310A>T	NCBI36
NG_012091.1:g.7570T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2673T>A	ENSP00000515567.1:p.Ile891=
ENST00000703937.1:c.*1734T>A	ENSP00000515568.1:n.*1734T>A
ENST00000326739.9:c.633T>A MANE Select	ENSP00000321584.4:p.Ile211=
ENST00000429182.6:c.633T>A	ENSP00000393525.2:p.Ile211=
ENST00000442157.2:c.558T>A	ENSP00000403502.2:p.Ile186=
ENST00000462980.2:n.1148T>A
ENST00000472328.2:n.699T>A
ENST00000491610.2:n.593T>A
ENST00000676607.1:n.929T>A
ENST00000676627.1:n.1363T>A
ENST00000676708.1:n.1913T>A
ENST00000676864.1:n.1782T>A
ENST00000677010.1:c.669T>A	ENSP00000503089.1:p.Ile223=
ENST00000677108.1:n.2539T>A
ENST00000677168.1:n.1105T>A
ENST00000677185.1:n.1196T>A
ENST00000677205.1:n.1417T>A
ENST00000677344.1:n.1907T>A
ENST00000677480.1:c.*310T>A	ENSP00000504378.1:n.*310T>A
ENST00000677519.1:n.1343T>A
ENST00000677593.1:n.1189T>A
ENST00000677740.1:n.2138T>A
ENST00000677991.1:n.1806T>A
ENST00000678001.1:n.1126T>A
ENST00000678085.1:n.1189T>A
ENST00000678177.1:n.2482T>A
ENST00000678603.1:n.1711T>A
ENST00000678724.1:c.558T>A	ENSP00000503874.1:p.Ile186=
ENST00000678920.1:n.791T>A
ENST00000679019.1:n.1403T>A
ENST00000679117.1:c.*448T>A	ENSP00000503240.1:n.*448T>A
ENST00000679339.1:n.1474T>A
ENST00000326739.8:c.633T>A	ENSP00000321584.4:p.Ile211=
ENST00000429182.5:c.427T>A
ENST00000442157.1:c.558T>A	ENSP00000403502.1:p.Ile186=
ENST00000462980.1:n.535T>A
ENST00000491610.1:n.593T>A
NM_000884.2:c.633T>A	NP_000875.2:p.Ile211=
XM_006713128.2:c.843T>A	XP_006713191.1:p.Ile281=
XM_006713128.3:c.843T>A	XP_006713191.1:p.Ile281=
XM_017006349.1:c.768T>A	XP_016861838.1:p.Ile256=
XM_017006350.1:c.768T>A	XP_016861839.1:p.Ile256=
NM_000884.3:c.633T>A MANE Select	NP_000875.2:p.Ile211=