Canonical Allele Identifier: CA433629596

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064237T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026804T>G , CM000665.2:g.49026804T>G	GRCh38
NC_000003.11:g.49064237T>G , CM000665.1:g.49064237T>G	GRCh37
NC_000003.10:g.49039241T>G	NCBI36
NG_012091.1:g.7639A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2742A>C	ENSP00000515567.1:p.Pro914=
ENST00000703937.1:c.*1803A>C	ENSP00000515568.1:n.*1803A>C
ENST00000326739.9:c.702A>C MANE Select	ENSP00000321584.4:p.Pro234=
ENST00000429182.6:c.702A>C	ENSP00000393525.2:p.Pro234=
ENST00000442157.2:c.627A>C	ENSP00000403502.2:p.Pro209=
ENST00000462980.2:n.1217A>C
ENST00000472328.2:n.768A>C
ENST00000491610.2:n.662A>C
ENST00000676607.1:n.998A>C
ENST00000676627.1:n.1432A>C
ENST00000676708.1:n.1982A>C
ENST00000676864.1:n.1851A>C
ENST00000677010.1:c.738A>C	ENSP00000503089.1:p.Pro246=
ENST00000677108.1:n.2608A>C
ENST00000677168.1:n.1174A>C
ENST00000677185.1:n.1265A>C
ENST00000677205.1:n.1486A>C
ENST00000677344.1:n.1976A>C
ENST00000677480.1:c.*379A>C	ENSP00000504378.1:n.*379A>C
ENST00000677519.1:n.1412A>C
ENST00000677593.1:n.1258A>C
ENST00000677740.1:n.2207A>C
ENST00000677991.1:n.1875A>C
ENST00000678001.1:n.1195A>C
ENST00000678085.1:n.1258A>C
ENST00000678177.1:n.2551A>C
ENST00000678603.1:n.1780A>C
ENST00000678724.1:c.627A>C	ENSP00000503874.1:p.Pro209=
ENST00000678920.1:n.860A>C
ENST00000679019.1:n.1472A>C
ENST00000679117.1:c.*517A>C	ENSP00000503240.1:n.*517A>C
ENST00000679339.1:n.1543A>C
ENST00000326739.8:c.702A>C	ENSP00000321584.4:p.Pro234=
ENST00000429182.5:c.496A>C
ENST00000442157.1:c.627A>C	ENSP00000403502.1:p.Pro209=
ENST00000462980.1:n.604A>C
ENST00000491610.1:n.662A>C
NM_000884.2:c.702A>C	NP_000875.2:p.Pro234=
XM_006713128.2:c.912A>C	XP_006713191.1:p.Pro304=
XM_006713128.3:c.912A>C	XP_006713191.1:p.Pro304=
XM_017006349.1:c.837A>C	XP_016861838.1:p.Pro279=
XM_017006350.1:c.837A>C	XP_016861839.1:p.Pro279=
NM_000884.3:c.702A>C MANE Select	NP_000875.2:p.Pro234=