Canonical Allele Identifier: CA433629524

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064171G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026738G>A , CM000665.2:g.49026738G>A	GRCh38
NC_000003.11:g.49064171G>A , CM000665.1:g.49064171G>A	GRCh37
NC_000003.10:g.49039175G>A	NCBI36
NG_012091.1:g.7705C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2808C>T	ENSP00000515567.1:p.Asp936=
ENST00000703937.1:c.*1869C>T	ENSP00000515568.1:n.*1869C>T
ENST00000326739.9:c.768C>T MANE Select	ENSP00000321584.4:p.Asp256=
ENST00000429182.6:c.768C>T	ENSP00000393525.2:p.Asp256=
ENST00000442157.2:c.693C>T	ENSP00000403502.2:p.Asp231=
ENST00000462980.2:n.1283C>T
ENST00000472328.2:n.834C>T
ENST00000491610.2:n.728C>T
ENST00000676607.1:n.1064C>T
ENST00000676627.1:n.1498C>T
ENST00000676708.1:n.2048C>T
ENST00000676864.1:n.1917C>T
ENST00000677010.1:c.804C>T	ENSP00000503089.1:p.Asp268=
ENST00000677108.1:n.2674C>T
ENST00000677168.1:n.1240C>T
ENST00000677185.1:n.1331C>T
ENST00000677205.1:n.1552C>T
ENST00000677344.1:n.2042C>T
ENST00000677480.1:c.*445C>T	ENSP00000504378.1:n.*445C>T
ENST00000677519.1:n.1478C>T
ENST00000677593.1:n.1324C>T
ENST00000677740.1:n.2273C>T
ENST00000677991.1:n.1941C>T
ENST00000678001.1:n.1261C>T
ENST00000678085.1:n.1324C>T
ENST00000678177.1:n.2617C>T
ENST00000678603.1:n.1846C>T
ENST00000678724.1:c.693C>T	ENSP00000503874.1:p.Asp231=
ENST00000678920.1:n.926C>T
ENST00000679019.1:n.1538C>T
ENST00000679117.1:c.*583C>T	ENSP00000503240.1:n.*583C>T
ENST00000679339.1:n.1609C>T
ENST00000326739.8:c.768C>T	ENSP00000321584.4:p.Asp256=
ENST00000429182.5:c.562C>T
ENST00000442157.1:c.693C>T	ENSP00000403502.1:p.Asp231=
ENST00000462980.1:n.670C>T
ENST00000491610.1:n.728C>T
NM_000884.2:c.768C>T	NP_000875.2:p.Asp256=
XM_006713128.2:c.978C>T	XP_006713191.1:p.Asp326=
XM_006713128.3:c.978C>T	XP_006713191.1:p.Asp326=
XM_017006349.1:c.903C>T	XP_016861838.1:p.Asp301=
XM_017006350.1:c.903C>T	XP_016861839.1:p.Asp301=
NM_000884.3:c.768C>T MANE Select	NP_000875.2:p.Asp256=