Canonical Allele Identifier: CA433629554

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064198C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026765C>A , CM000665.2:g.49026765C>A	GRCh38
NC_000003.11:g.49064198C>A , CM000665.1:g.49064198C>A	GRCh37
NC_000003.10:g.49039202C>A	NCBI36
NG_012091.1:g.7678G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2781G>T	ENSP00000515567.1:p.Gly927=
ENST00000703937.1:c.*1842G>T	ENSP00000515568.1:n.*1842G>T
ENST00000326739.9:c.741G>T MANE Select	ENSP00000321584.4:p.Gly247=
ENST00000429182.6:c.741G>T	ENSP00000393525.2:p.Gly247=
ENST00000442157.2:c.666G>T	ENSP00000403502.2:p.Gly222=
ENST00000462980.2:n.1256G>T
ENST00000472328.2:n.807G>T
ENST00000491610.2:n.701G>T
ENST00000676607.1:n.1037G>T
ENST00000676627.1:n.1471G>T
ENST00000676708.1:n.2021G>T
ENST00000676864.1:n.1890G>T
ENST00000677010.1:c.777G>T	ENSP00000503089.1:p.Gly259=
ENST00000677108.1:n.2647G>T
ENST00000677168.1:n.1213G>T
ENST00000677185.1:n.1304G>T
ENST00000677205.1:n.1525G>T
ENST00000677344.1:n.2015G>T
ENST00000677480.1:c.*418G>T	ENSP00000504378.1:n.*418G>T
ENST00000677519.1:n.1451G>T
ENST00000677593.1:n.1297G>T
ENST00000677740.1:n.2246G>T
ENST00000677991.1:n.1914G>T
ENST00000678001.1:n.1234G>T
ENST00000678085.1:n.1297G>T
ENST00000678177.1:n.2590G>T
ENST00000678603.1:n.1819G>T
ENST00000678724.1:c.666G>T	ENSP00000503874.1:p.Gly222=
ENST00000678920.1:n.899G>T
ENST00000679019.1:n.1511G>T
ENST00000679117.1:c.*556G>T	ENSP00000503240.1:n.*556G>T
ENST00000679339.1:n.1582G>T
ENST00000326739.8:c.741G>T	ENSP00000321584.4:p.Gly247=
ENST00000429182.5:c.535G>T
ENST00000442157.1:c.666G>T	ENSP00000403502.1:p.Gly222=
ENST00000462980.1:n.643G>T
ENST00000491610.1:n.701G>T
NM_000884.2:c.741G>T	NP_000875.2:p.Gly247=
XM_006713128.2:c.951G>T	XP_006713191.1:p.Gly317=
XM_006713128.3:c.951G>T	XP_006713191.1:p.Gly317=
XM_017006349.1:c.876G>T	XP_016861838.1:p.Gly292=
XM_017006350.1:c.876G>T	XP_016861839.1:p.Gly292=
NM_000884.3:c.741G>T MANE Select	NP_000875.2:p.Gly247=