Canonical Allele Identifier: CA1363291745
Gene: IMPDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026956T= , CM000665.2:g.49026956T= GRCh38
NC_000003.11:g.49064389T= , CM000665.1:g.49064389T= GRCh37
NC_000003.10:g.49039393T= NCBI36
NG_012091.1:g.7487A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2659+4A= ENSP00000515567.1:n.2659+4A=
ENST00000703937.1:c.*1720+4A= ENSP00000515568.1:n.*1720+4A=
ENST00000326739.9:c.619+4A= MANE Select ENSP00000321584.4:n.619+4A=
ENST00000429182.6:c.619+4A= ENSP00000393525.2:n.619+4A=
ENST00000442157.2:c.544+4A= ENSP00000403502.2:n.544+4A=
ENST00000462980.2:n.1134+4A=
ENST00000472328.2:n.685+4A=
ENST00000491610.2:n.510A=
ENST00000676607.1:n.915+4A=
ENST00000676627.1:n.1349+4A=
ENST00000676708.1:n.1830A=
ENST00000676864.1:n.1699A=
ENST00000677010.1:c.655+4A= ENSP00000503089.1:n.655+4A=
ENST00000677108.1:n.2456A=
ENST00000677168.1:n.1091+4A=
ENST00000677185.1:n.1113A=
ENST00000677205.1:n.1334A=
ENST00000677344.1:n.1824A=
ENST00000677480.1:c.*296+4A= ENSP00000504378.1:n.*296+4A=
ENST00000677519.1:n.1329+4A=
ENST00000677593.1:n.1106A=
ENST00000677740.1:n.2055A=
ENST00000677991.1:n.1792+4A=
ENST00000678001.1:n.1112+4A=
ENST00000678085.1:n.1106A=
ENST00000678177.1:n.2399A=
ENST00000678603.1:n.1697+4A=
ENST00000678724.1:c.544+4A= ENSP00000503874.1:n.544+4A=
ENST00000678920.1:n.777+4A=
ENST00000679019.1:n.1320A=
ENST00000679117.1:c.*434+4A= ENSP00000503240.1:n.*434+4A=
ENST00000679339.1:n.1391A=
ENST00000326739.8:c.619+4A= ENSP00000321584.4:n.619+4A=
ENST00000429182.5:c.413+4A=
ENST00000442157.1:c.544+4A= ENSP00000403502.1:n.544+4A=
ENST00000462980.1:n.521+4A=
ENST00000491610.1:n.510A=
NM_000884.2:c.619+4A= NP_000875.2:n.619+4A=
XM_006713128.2:c.829+4A= XP_006713191.1:n.829+4A=
XM_006713128.3:c.829+4A= XP_006713191.1:n.829+4A=
XM_017006349.1:c.754+4A= XP_016861838.1:n.754+4A=
XM_017006350.1:c.754+4A= XP_016861839.1:n.754+4A=
NM_000884.3:c.619+4A= MANE Select NP_000875.2:n.619+4A=