Canonical Allele Identifier: CA433629637

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064264T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026831T>G , CM000665.2:g.49026831T>G	GRCh38
NC_000003.11:g.49064264T>G , CM000665.1:g.49064264T>G	GRCh37
NC_000003.10:g.49039268T>G	NCBI36
NG_012091.1:g.7612A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2715A>C	ENSP00000515567.1:p.Thr905=
ENST00000703937.1:c.*1776A>C	ENSP00000515568.1:n.*1776A>C
ENST00000326739.9:c.675A>C MANE Select	ENSP00000321584.4:p.Thr225=
ENST00000429182.6:c.675A>C	ENSP00000393525.2:p.Thr225=
ENST00000442157.2:c.600A>C	ENSP00000403502.2:p.Thr200=
ENST00000462980.2:n.1190A>C
ENST00000472328.2:n.741A>C
ENST00000491610.2:n.635A>C
ENST00000676607.1:n.971A>C
ENST00000676627.1:n.1405A>C
ENST00000676708.1:n.1955A>C
ENST00000676864.1:n.1824A>C
ENST00000677010.1:c.711A>C	ENSP00000503089.1:p.Thr237=
ENST00000677108.1:n.2581A>C
ENST00000677168.1:n.1147A>C
ENST00000677185.1:n.1238A>C
ENST00000677205.1:n.1459A>C
ENST00000677344.1:n.1949A>C
ENST00000677480.1:c.*352A>C	ENSP00000504378.1:n.*352A>C
ENST00000677519.1:n.1385A>C
ENST00000677593.1:n.1231A>C
ENST00000677740.1:n.2180A>C
ENST00000677991.1:n.1848A>C
ENST00000678001.1:n.1168A>C
ENST00000678085.1:n.1231A>C
ENST00000678177.1:n.2524A>C
ENST00000678603.1:n.1753A>C
ENST00000678724.1:c.600A>C	ENSP00000503874.1:p.Thr200=
ENST00000678920.1:n.833A>C
ENST00000679019.1:n.1445A>C
ENST00000679117.1:c.*490A>C	ENSP00000503240.1:n.*490A>C
ENST00000679339.1:n.1516A>C
ENST00000326739.8:c.675A>C	ENSP00000321584.4:p.Thr225=
ENST00000429182.5:c.469A>C
ENST00000442157.1:c.600A>C	ENSP00000403502.1:p.Thr200=
ENST00000462980.1:n.577A>C
ENST00000491610.1:n.635A>C
NM_000884.2:c.675A>C	NP_000875.2:p.Thr225=
XM_006713128.2:c.885A>C	XP_006713191.1:p.Thr295=
XM_006713128.3:c.885A>C	XP_006713191.1:p.Thr295=
XM_017006349.1:c.810A>C	XP_016861838.1:p.Thr270=
XM_017006350.1:c.810A>C	XP_016861839.1:p.Thr270=
NM_000884.3:c.675A>C MANE Select	NP_000875.2:p.Thr225=