Canonical Allele Identifier: CA433629657

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064270G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026837G>C , CM000665.2:g.49026837G>C	GRCh38
NC_000003.11:g.49064270G>C , CM000665.1:g.49064270G>C	GRCh37
NC_000003.10:g.49039274G>C	NCBI36
NG_012091.1:g.7606C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2709C>G	ENSP00000515567.1:p.Ala903=
ENST00000703937.1:c.*1770C>G	ENSP00000515568.1:n.*1770C>G
ENST00000326739.9:c.669C>G MANE Select	ENSP00000321584.4:p.Ala223=
ENST00000429182.6:c.669C>G	ENSP00000393525.2:p.Ala223=
ENST00000442157.2:c.594C>G	ENSP00000403502.2:p.Ala198=
ENST00000462980.2:n.1184C>G
ENST00000472328.2:n.735C>G
ENST00000491610.2:n.629C>G
ENST00000676607.1:n.965C>G
ENST00000676627.1:n.1399C>G
ENST00000676708.1:n.1949C>G
ENST00000676864.1:n.1818C>G
ENST00000677010.1:c.705C>G	ENSP00000503089.1:p.Ala235=
ENST00000677108.1:n.2575C>G
ENST00000677168.1:n.1141C>G
ENST00000677185.1:n.1232C>G
ENST00000677205.1:n.1453C>G
ENST00000677344.1:n.1943C>G
ENST00000677480.1:c.*346C>G	ENSP00000504378.1:n.*346C>G
ENST00000677519.1:n.1379C>G
ENST00000677593.1:n.1225C>G
ENST00000677740.1:n.2174C>G
ENST00000677991.1:n.1842C>G
ENST00000678001.1:n.1162C>G
ENST00000678085.1:n.1225C>G
ENST00000678177.1:n.2518C>G
ENST00000678603.1:n.1747C>G
ENST00000678724.1:c.594C>G	ENSP00000503874.1:p.Ala198=
ENST00000678920.1:n.827C>G
ENST00000679019.1:n.1439C>G
ENST00000679117.1:c.*484C>G	ENSP00000503240.1:n.*484C>G
ENST00000679339.1:n.1510C>G
ENST00000326739.8:c.669C>G	ENSP00000321584.4:p.Ala223=
ENST00000429182.5:c.463C>G
ENST00000442157.1:c.594C>G	ENSP00000403502.1:p.Ala198=
ENST00000462980.1:n.571C>G
ENST00000491610.1:n.629C>G
NM_000884.2:c.669C>G	NP_000875.2:p.Ala223=
XM_006713128.2:c.879C>G	XP_006713191.1:p.Ala293=
XM_006713128.3:c.879C>G	XP_006713191.1:p.Ala293=
XM_017006349.1:c.804C>G	XP_016861838.1:p.Ala268=
XM_017006350.1:c.804C>G	XP_016861839.1:p.Ala268=
NM_000884.3:c.669C>G MANE Select	NP_000875.2:p.Ala223=