Canonical Allele Identifier: CA433629358

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064028T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026595T>A , CM000665.2:g.49026595T>A	GRCh38
NC_000003.11:g.49064028T>A , CM000665.1:g.49064028T>A	GRCh37
NC_000003.10:g.49039032T>A	NCBI36
NG_012091.1:g.7848A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2874A>T	ENSP00000515567.1:p.Gly958=
ENST00000703937.1:c.*1935A>T	ENSP00000515568.1:n.*1935A>T
ENST00000326739.9:c.834A>T MANE Select	ENSP00000321584.4:p.Gly278=
ENST00000429182.6:c.834A>T	ENSP00000393525.2:p.Gly278=
ENST00000442157.2:c.759A>T	ENSP00000403502.2:p.Gly253=
ENST00000462980.2:n.1349A>T
ENST00000472328.2:n.900A>T
ENST00000491610.2:n.794A>T
ENST00000676607.1:n.1130A>T
ENST00000676627.1:n.1564A>T
ENST00000676708.1:n.2114A>T
ENST00000676864.1:n.1983A>T
ENST00000677010.1:c.858A>T	ENSP00000503089.1:p.Gly286=
ENST00000677108.1:n.2817A>T
ENST00000677168.1:n.1306A>T
ENST00000677185.1:n.1397A>T
ENST00000677205.1:n.1618A>T
ENST00000677344.1:n.2108A>T
ENST00000677480.1:c.*511A>T	ENSP00000504378.1:n.*511A>T
ENST00000677519.1:n.1544A>T
ENST00000677593.1:n.1390A>T
ENST00000677740.1:n.2339A>T
ENST00000677991.1:n.2007A>T
ENST00000678001.1:n.1327A>T
ENST00000678085.1:n.1467A>T
ENST00000678177.1:n.2760A>T
ENST00000678603.1:n.1912A>T
ENST00000678724.1:c.759A>T	ENSP00000503874.1:p.Gly253=
ENST00000678920.1:n.992A>T
ENST00000679019.1:n.1681A>T
ENST00000679117.1:c.*649A>T	ENSP00000503240.1:n.*649A>T
ENST00000679339.1:n.1675A>T
ENST00000326739.8:c.834A>T	ENSP00000321584.4:p.Gly278=
ENST00000429182.5:c.628A>T
ENST00000442157.1:c.759A>T	ENSP00000403502.1:p.Gly253=
ENST00000462980.1:n.736A>T
ENST00000491610.1:n.794A>T
NM_000884.2:c.834A>T	NP_000875.2:p.Gly278=
XM_006713128.2:c.1044A>T	XP_006713191.1:p.Gly348=
XM_006713128.3:c.1044A>T	XP_006713191.1:p.Gly348=
XM_017006349.1:c.969A>T	XP_016861838.1:p.Gly323=
XM_017006350.1:c.969A>T	XP_016861839.1:p.Gly323=
NM_000884.3:c.834A>T MANE Select	NP_000875.2:p.Gly278=