Canonical Allele Identifier: CA1363291717
Gene: IMPDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026914G= , CM000665.2:g.49026914G= GRCh38
NC_000003.11:g.49064347G= , CM000665.1:g.49064347G= GRCh37
NC_000003.10:g.49039351G= NCBI36
NG_012091.1:g.7529C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2660-28C= ENSP00000515567.1:n.2660-28C=
ENST00000703937.1:c.*1721-28C= ENSP00000515568.1:n.*1721-28C=
ENST00000326739.9:c.620-28C= MANE Select ENSP00000321584.4:n.620-28C=
ENST00000429182.6:c.620-28C= ENSP00000393525.2:n.620-28C=
ENST00000442157.2:c.545-28C= ENSP00000403502.2:n.545-28C=
ENST00000462980.2:n.1135-28C=
ENST00000472328.2:n.686-28C=
ENST00000491610.2:n.552C=
ENST00000676607.1:n.916-28C=
ENST00000676627.1:n.1350-28C=
ENST00000676708.1:n.1872C=
ENST00000676864.1:n.1741C=
ENST00000677010.1:c.656-28C= ENSP00000503089.1:n.656-28C=
ENST00000677108.1:n.2498C=
ENST00000677168.1:n.1092-28C=
ENST00000677185.1:n.1155C=
ENST00000677205.1:n.1376C=
ENST00000677344.1:n.1866C=
ENST00000677480.1:c.*297-28C= ENSP00000504378.1:n.*297-28C=
ENST00000677519.1:n.1330-28C=
ENST00000677593.1:n.1148C=
ENST00000677740.1:n.2097C=
ENST00000677991.1:n.1793-28C=
ENST00000678001.1:n.1113-28C=
ENST00000678085.1:n.1148C=
ENST00000678177.1:n.2441C=
ENST00000678603.1:n.1698-28C=
ENST00000678724.1:c.545-28C= ENSP00000503874.1:n.545-28C=
ENST00000678920.1:n.778-28C=
ENST00000679019.1:n.1362C=
ENST00000679117.1:c.*435-28C= ENSP00000503240.1:n.*435-28C=
ENST00000679339.1:n.1433C=
ENST00000326739.8:c.620-28C= ENSP00000321584.4:n.620-28C=
ENST00000429182.5:c.414-28C=
ENST00000442157.1:c.545-28C= ENSP00000403502.1:n.545-28C=
ENST00000462980.1:n.522-28C=
ENST00000491610.1:n.552C=
NM_000884.2:c.620-28C= NP_000875.2:n.620-28C=
XM_006713128.2:c.830-28C= XP_006713191.1:n.830-28C=
XM_006713128.3:c.830-28C= XP_006713191.1:n.830-28C=
XM_017006349.1:c.755-28C= XP_016861838.1:n.755-28C=
XM_017006350.1:c.755-28C= XP_016861839.1:n.755-28C=
NM_000884.3:c.620-28C= MANE Select NP_000875.2:n.620-28C=