Canonical Allele Identifier: CA352740592
Gene: IMPDH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026810G>T , CM000665.2:g.49026810G>T GRCh38
NC_000003.11:g.49064243G>T , CM000665.1:g.49064243G>T GRCh37
NC_000003.10:g.49039247G>T NCBI36
NG_012091.1:g.7633C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2736C>A ENSP00000515567.1:p.Asp912Glu
ENST00000703937.1:c.*1797C>A ENSP00000515568.1:n.*1797C>A
ENST00000326739.9:c.696C>A MANE Select ENSP00000321584.4:p.Asp232Glu
ENST00000429182.6:c.696C>A ENSP00000393525.2:p.Asp232Glu
ENST00000442157.2:c.621C>A ENSP00000403502.2:p.Asp207Glu
ENST00000462980.2:n.1211C>A
ENST00000472328.2:n.762C>A
ENST00000491610.2:n.656C>A
ENST00000676607.1:n.992C>A
ENST00000676627.1:n.1426C>A
ENST00000676708.1:n.1976C>A
ENST00000676864.1:n.1845C>A
ENST00000677010.1:c.732C>A ENSP00000503089.1:p.Asp244Glu
ENST00000677108.1:n.2602C>A
ENST00000677168.1:n.1168C>A
ENST00000677185.1:n.1259C>A
ENST00000677205.1:n.1480C>A
ENST00000677344.1:n.1970C>A
ENST00000677480.1:c.*373C>A ENSP00000504378.1:n.*373C>A
ENST00000677519.1:n.1406C>A
ENST00000677593.1:n.1252C>A
ENST00000677740.1:n.2201C>A
ENST00000677991.1:n.1869C>A
ENST00000678001.1:n.1189C>A
ENST00000678085.1:n.1252C>A
ENST00000678177.1:n.2545C>A
ENST00000678603.1:n.1774C>A
ENST00000678724.1:c.621C>A ENSP00000503874.1:p.Asp207Glu
ENST00000678920.1:n.854C>A
ENST00000679019.1:n.1466C>A
ENST00000679117.1:c.*511C>A ENSP00000503240.1:n.*511C>A
ENST00000679339.1:n.1537C>A
ENST00000326739.8:c.696C>A ENSP00000321584.4:p.Asp232Glu
ENST00000429182.5:c.490C>A
ENST00000442157.1:c.621C>A ENSP00000403502.1:p.Asp207Glu
ENST00000462980.1:n.598C>A
ENST00000491610.1:n.656C>A
NM_000884.2:c.696C>A NP_000875.2:p.Asp232Glu
XM_006713128.2:c.906C>A XP_006713191.1:p.Asp302Glu
XM_006713128.3:c.906C>A XP_006713191.1:p.Asp302Glu
XM_017006349.1:c.831C>A XP_016861838.1:p.Asp277Glu
XM_017006350.1:c.831C>A XP_016861839.1:p.Asp277Glu
NM_000884.3:c.696C>A MANE Select NP_000875.2:p.Asp232Glu