Canonical Allele Identifier: CA433629566

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064207C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026774C>T , CM000665.2:g.49026774C>T	GRCh38
NC_000003.11:g.49064207C>T , CM000665.1:g.49064207C>T	GRCh37
NC_000003.10:g.49039211C>T	NCBI36
NG_012091.1:g.7669G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2772G>A	ENSP00000515567.1:p.Leu924=
ENST00000703937.1:c.*1833G>A	ENSP00000515568.1:n.*1833G>A
ENST00000326739.9:c.732G>A MANE Select	ENSP00000321584.4:p.Leu244=
ENST00000429182.6:c.732G>A	ENSP00000393525.2:p.Leu244=
ENST00000442157.2:c.657G>A	ENSP00000403502.2:p.Leu219=
ENST00000462980.2:n.1247G>A
ENST00000472328.2:n.798G>A
ENST00000491610.2:n.692G>A
ENST00000676607.1:n.1028G>A
ENST00000676627.1:n.1462G>A
ENST00000676708.1:n.2012G>A
ENST00000676864.1:n.1881G>A
ENST00000677010.1:c.768G>A	ENSP00000503089.1:p.Leu256=
ENST00000677108.1:n.2638G>A
ENST00000677168.1:n.1204G>A
ENST00000677185.1:n.1295G>A
ENST00000677205.1:n.1516G>A
ENST00000677344.1:n.2006G>A
ENST00000677480.1:c.*409G>A	ENSP00000504378.1:n.*409G>A
ENST00000677519.1:n.1442G>A
ENST00000677593.1:n.1288G>A
ENST00000677740.1:n.2237G>A
ENST00000677991.1:n.1905G>A
ENST00000678001.1:n.1225G>A
ENST00000678085.1:n.1288G>A
ENST00000678177.1:n.2581G>A
ENST00000678603.1:n.1810G>A
ENST00000678724.1:c.657G>A	ENSP00000503874.1:p.Leu219=
ENST00000678920.1:n.890G>A
ENST00000679019.1:n.1502G>A
ENST00000679117.1:c.*547G>A	ENSP00000503240.1:n.*547G>A
ENST00000679339.1:n.1573G>A
ENST00000326739.8:c.732G>A	ENSP00000321584.4:p.Leu244=
ENST00000429182.5:c.526G>A
ENST00000442157.1:c.657G>A	ENSP00000403502.1:p.Leu219=
ENST00000462980.1:n.634G>A
ENST00000491610.1:n.692G>A
NM_000884.2:c.732G>A	NP_000875.2:p.Leu244=
XM_006713128.2:c.942G>A	XP_006713191.1:p.Leu314=
XM_006713128.3:c.942G>A	XP_006713191.1:p.Leu314=
XM_017006349.1:c.867G>A	XP_016861838.1:p.Leu289=
XM_017006350.1:c.867G>A	XP_016861839.1:p.Leu289=
NM_000884.3:c.732G>A MANE Select	NP_000875.2:p.Leu244=