Canonical Allele Identifier: CA433629604

Gene: IMPDH2

Linked Data

• dbSNP Id: rs1575310234
• MyVariant Identifiers: chr3:g.49064243G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026810G>A , CM000665.2:g.49026810G>A	GRCh38
NC_000003.11:g.49064243G>A , CM000665.1:g.49064243G>A	GRCh37
NC_000003.10:g.49039247G>A	NCBI36
NG_012091.1:g.7633C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2736C>T	ENSP00000515567.1:p.Asp912=
ENST00000703937.1:c.*1797C>T	ENSP00000515568.1:n.*1797C>T
ENST00000326739.9:c.696C>T MANE Select	ENSP00000321584.4:p.Asp232=
ENST00000429182.6:c.696C>T	ENSP00000393525.2:p.Asp232=
ENST00000442157.2:c.621C>T	ENSP00000403502.2:p.Asp207=
ENST00000462980.2:n.1211C>T
ENST00000472328.2:n.762C>T
ENST00000491610.2:n.656C>T
ENST00000676607.1:n.992C>T
ENST00000676627.1:n.1426C>T
ENST00000676708.1:n.1976C>T
ENST00000676864.1:n.1845C>T
ENST00000677010.1:c.732C>T	ENSP00000503089.1:p.Asp244=
ENST00000677108.1:n.2602C>T
ENST00000677168.1:n.1168C>T
ENST00000677185.1:n.1259C>T
ENST00000677205.1:n.1480C>T
ENST00000677344.1:n.1970C>T
ENST00000677480.1:c.*373C>T	ENSP00000504378.1:n.*373C>T
ENST00000677519.1:n.1406C>T
ENST00000677593.1:n.1252C>T
ENST00000677740.1:n.2201C>T
ENST00000677991.1:n.1869C>T
ENST00000678001.1:n.1189C>T
ENST00000678085.1:n.1252C>T
ENST00000678177.1:n.2545C>T
ENST00000678603.1:n.1774C>T
ENST00000678724.1:c.621C>T	ENSP00000503874.1:p.Asp207=
ENST00000678920.1:n.854C>T
ENST00000679019.1:n.1466C>T
ENST00000679117.1:c.*511C>T	ENSP00000503240.1:n.*511C>T
ENST00000679339.1:n.1537C>T
ENST00000326739.8:c.696C>T	ENSP00000321584.4:p.Asp232=
ENST00000429182.5:c.490C>T
ENST00000442157.1:c.621C>T	ENSP00000403502.1:p.Asp207=
ENST00000462980.1:n.598C>T
ENST00000491610.1:n.656C>T
NM_000884.2:c.696C>T	NP_000875.2:p.Asp232=
XM_006713128.2:c.906C>T	XP_006713191.1:p.Asp302=
XM_006713128.3:c.906C>T	XP_006713191.1:p.Asp302=
XM_017006349.1:c.831C>T	XP_016861838.1:p.Asp277=
XM_017006350.1:c.831C>T	XP_016861839.1:p.Asp277=
NM_000884.3:c.696C>T MANE Select	NP_000875.2:p.Asp232=