Canonical Allele Identifier: CA433629717

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064309G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026876G>T , CM000665.2:g.49026876G>T	GRCh38
NC_000003.11:g.49064309G>T , CM000665.1:g.49064309G>T	GRCh37
NC_000003.10:g.49039313G>T	NCBI36
NG_012091.1:g.7567C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2670C>A	ENSP00000515567.1:p.Pro890=
ENST00000703937.1:c.*1731C>A	ENSP00000515568.1:n.*1731C>A
ENST00000326739.9:c.630C>A MANE Select	ENSP00000321584.4:p.Pro210=
ENST00000429182.6:c.630C>A	ENSP00000393525.2:p.Pro210=
ENST00000442157.2:c.555C>A	ENSP00000403502.2:p.Pro185=
ENST00000462980.2:n.1145C>A
ENST00000472328.2:n.696C>A
ENST00000491610.2:n.590C>A
ENST00000676607.1:n.926C>A
ENST00000676627.1:n.1360C>A
ENST00000676708.1:n.1910C>A
ENST00000676864.1:n.1779C>A
ENST00000677010.1:c.666C>A	ENSP00000503089.1:p.Pro222=
ENST00000677108.1:n.2536C>A
ENST00000677168.1:n.1102C>A
ENST00000677185.1:n.1193C>A
ENST00000677205.1:n.1414C>A
ENST00000677344.1:n.1904C>A
ENST00000677480.1:c.*307C>A	ENSP00000504378.1:n.*307C>A
ENST00000677519.1:n.1340C>A
ENST00000677593.1:n.1186C>A
ENST00000677740.1:n.2135C>A
ENST00000677991.1:n.1803C>A
ENST00000678001.1:n.1123C>A
ENST00000678085.1:n.1186C>A
ENST00000678177.1:n.2479C>A
ENST00000678603.1:n.1708C>A
ENST00000678724.1:c.555C>A	ENSP00000503874.1:p.Pro185=
ENST00000678920.1:n.788C>A
ENST00000679019.1:n.1400C>A
ENST00000679117.1:c.*445C>A	ENSP00000503240.1:n.*445C>A
ENST00000679339.1:n.1471C>A
ENST00000326739.8:c.630C>A	ENSP00000321584.4:p.Pro210=
ENST00000429182.5:c.424C>A
ENST00000442157.1:c.555C>A	ENSP00000403502.1:p.Pro185=
ENST00000462980.1:n.532C>A
ENST00000491610.1:n.590C>A
NM_000884.2:c.630C>A	NP_000875.2:p.Pro210=
XM_006713128.2:c.840C>A	XP_006713191.1:p.Pro280=
XM_006713128.3:c.840C>A	XP_006713191.1:p.Pro280=
XM_017006349.1:c.765C>A	XP_016861838.1:p.Pro255=
XM_017006350.1:c.765C>A	XP_016861839.1:p.Pro255=
NM_000884.3:c.630C>A MANE Select	NP_000875.2:p.Pro210=