Canonical Allele Identifier: CA433629511

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064155A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026722A>G , CM000665.2:g.49026722A>G	GRCh38
NC_000003.11:g.49064155A>G , CM000665.1:g.49064155A>G	GRCh37
NC_000003.10:g.49039159A>G	NCBI36
NG_012091.1:g.7721T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2824T>C	ENSP00000515567.1:p.Leu942=
ENST00000703937.1:c.*1885T>C	ENSP00000515568.1:n.*1885T>C
ENST00000326739.9:c.784T>C MANE Select	ENSP00000321584.4:p.Leu262=
ENST00000429182.6:c.784T>C	ENSP00000393525.2:p.Leu262=
ENST00000442157.2:c.709T>C	ENSP00000403502.2:p.Leu237=
ENST00000462980.2:n.1299T>C
ENST00000472328.2:n.850T>C
ENST00000491610.2:n.744T>C
ENST00000676607.1:n.1080T>C
ENST00000676627.1:n.1514T>C
ENST00000676708.1:n.2064T>C
ENST00000676864.1:n.1933T>C
ENST00000677010.1:c.820T>C	ENSP00000503089.1:p.Leu274=
ENST00000677108.1:n.2690T>C
ENST00000677168.1:n.1256T>C
ENST00000677185.1:n.1347T>C
ENST00000677205.1:n.1568T>C
ENST00000677344.1:n.2058T>C
ENST00000677480.1:c.*461T>C	ENSP00000504378.1:n.*461T>C
ENST00000677519.1:n.1494T>C
ENST00000677593.1:n.1340T>C
ENST00000677740.1:n.2289T>C
ENST00000677991.1:n.1957T>C
ENST00000678001.1:n.1277T>C
ENST00000678085.1:n.1340T>C
ENST00000678177.1:n.2633T>C
ENST00000678603.1:n.1862T>C
ENST00000678724.1:c.709T>C	ENSP00000503874.1:p.Leu237=
ENST00000678920.1:n.942T>C
ENST00000679019.1:n.1554T>C
ENST00000679117.1:c.*599T>C	ENSP00000503240.1:n.*599T>C
ENST00000679339.1:n.1625T>C
ENST00000326739.8:c.784T>C	ENSP00000321584.4:p.Leu262=
ENST00000429182.5:c.578T>C
ENST00000442157.1:c.709T>C	ENSP00000403502.1:p.Leu237=
ENST00000462980.1:n.686T>C
ENST00000491610.1:n.744T>C
NM_000884.2:c.784T>C	NP_000875.2:p.Leu262=
XM_006713128.2:c.994T>C	XP_006713191.1:p.Leu332=
XM_006713128.3:c.994T>C	XP_006713191.1:p.Leu332=
XM_017006349.1:c.919T>C	XP_016861838.1:p.Leu307=
XM_017006350.1:c.919T>C	XP_016861839.1:p.Leu307=
NM_000884.3:c.784T>C MANE Select	NP_000875.2:p.Leu262=