Canonical Allele Identifier: CA352740796
Gene: IMPDH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026833T>A , CM000665.2:g.49026833T>A GRCh38
NC_000003.11:g.49064266T>A , CM000665.1:g.49064266T>A GRCh37
NC_000003.10:g.49039270T>A NCBI36
NG_012091.1:g.7610A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2713A>T ENSP00000515567.1:p.Thr905Ser
ENST00000703937.1:c.*1774A>T ENSP00000515568.1:n.*1774A>T
ENST00000326739.9:c.673A>T MANE Select ENSP00000321584.4:p.Thr225Ser
ENST00000429182.6:c.673A>T ENSP00000393525.2:p.Thr225Ser
ENST00000442157.2:c.598A>T ENSP00000403502.2:p.Thr200Ser
ENST00000462980.2:n.1188A>T
ENST00000472328.2:n.739A>T
ENST00000491610.2:n.633A>T
ENST00000676607.1:n.969A>T
ENST00000676627.1:n.1403A>T
ENST00000676708.1:n.1953A>T
ENST00000676864.1:n.1822A>T
ENST00000677010.1:c.709A>T ENSP00000503089.1:p.Thr237Ser
ENST00000677108.1:n.2579A>T
ENST00000677168.1:n.1145A>T
ENST00000677185.1:n.1236A>T
ENST00000677205.1:n.1457A>T
ENST00000677344.1:n.1947A>T
ENST00000677480.1:c.*350A>T ENSP00000504378.1:n.*350A>T
ENST00000677519.1:n.1383A>T
ENST00000677593.1:n.1229A>T
ENST00000677740.1:n.2178A>T
ENST00000677991.1:n.1846A>T
ENST00000678001.1:n.1166A>T
ENST00000678085.1:n.1229A>T
ENST00000678177.1:n.2522A>T
ENST00000678603.1:n.1751A>T
ENST00000678724.1:c.598A>T ENSP00000503874.1:p.Thr200Ser
ENST00000678920.1:n.831A>T
ENST00000679019.1:n.1443A>T
ENST00000679117.1:c.*488A>T ENSP00000503240.1:n.*488A>T
ENST00000679339.1:n.1514A>T
ENST00000326739.8:c.673A>T ENSP00000321584.4:p.Thr225Ser
ENST00000429182.5:c.467A>T
ENST00000442157.1:c.598A>T ENSP00000403502.1:p.Thr200Ser
ENST00000462980.1:n.575A>T
ENST00000491610.1:n.633A>T
NM_000884.2:c.673A>T NP_000875.2:p.Thr225Ser
XM_006713128.2:c.883A>T XP_006713191.1:p.Thr295Ser
XM_006713128.3:c.883A>T XP_006713191.1:p.Thr295Ser
XM_017006349.1:c.808A>T XP_016861838.1:p.Thr270Ser
XM_017006350.1:c.808A>T XP_016861839.1:p.Thr270Ser
NM_000884.3:c.673A>T MANE Select NP_000875.2:p.Thr225Ser