Canonical Allele Identifier: CA352739840

Gene: IMPDH2

Linked Data

• dbSNP Id: rs1575310113
• MyVariant Identifiers: chr3:g.49064131C>T (hg19) ; chr3:g.49026698C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026698C>T , CM000665.2:g.49026698C>T	GRCh38
NC_000003.11:g.49064131C>T , CM000665.1:g.49064131C>T	GRCh37
NC_000003.10:g.49039135C>T	NCBI36
NG_012091.1:g.7745G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2848G>A	ENSP00000515567.1:p.Val950Ile
ENST00000703937.1:c.*1909G>A	ENSP00000515568.1:n.*1909G>A
ENST00000326739.9:c.808G>A MANE Select	ENSP00000321584.4:p.Val270Ile
ENST00000429182.6:c.808G>A	ENSP00000393525.2:p.Val270Ile
ENST00000442157.2:c.733G>A	ENSP00000403502.2:p.Val245Ile
ENST00000462980.2:n.1323G>A
ENST00000472328.2:n.874G>A
ENST00000491610.2:n.768G>A
ENST00000676607.1:n.1104G>A
ENST00000676627.1:n.1538G>A
ENST00000676708.1:n.2088G>A
ENST00000676864.1:n.1957G>A
ENST00000677010.1:c.844G>A	ENSP00000503089.1:p.Val282Ile
ENST00000677108.1:n.2714G>A
ENST00000677168.1:n.1280G>A
ENST00000677185.1:n.1371G>A
ENST00000677205.1:n.1592G>A
ENST00000677344.1:n.2082G>A
ENST00000677480.1:c.*485G>A	ENSP00000504378.1:n.*485G>A
ENST00000677519.1:n.1518G>A
ENST00000677593.1:n.1364G>A
ENST00000677740.1:n.2313G>A
ENST00000677991.1:n.1981G>A
ENST00000678001.1:n.1301G>A
ENST00000678085.1:n.1364G>A
ENST00000678177.1:n.2657G>A
ENST00000678603.1:n.1886G>A
ENST00000678724.1:c.733G>A	ENSP00000503874.1:p.Val245Ile
ENST00000678920.1:n.966G>A
ENST00000679019.1:n.1578G>A
ENST00000679117.1:c.*623G>A	ENSP00000503240.1:n.*623G>A
ENST00000679339.1:n.1649G>A
ENST00000326739.8:c.808G>A	ENSP00000321584.4:p.Val270Ile
ENST00000429182.5:c.602G>A
ENST00000442157.1:c.733G>A	ENSP00000403502.1:p.Val245Ile
ENST00000462980.1:n.710G>A
ENST00000491610.1:n.768G>A
NM_000884.2:c.808G>A	NP_000875.2:p.Val270Ile
XM_006713128.2:c.1018G>A	XP_006713191.1:p.Val340Ile
XM_006713128.3:c.1018G>A	XP_006713191.1:p.Val340Ile
XM_017006349.1:c.943G>A	XP_016861838.1:p.Val315Ile
XM_017006350.1:c.943G>A	XP_016861839.1:p.Val315Ile
NM_000884.3:c.808G>A MANE Select	NP_000875.2:p.Val270Ile