Canonical Allele Identifier: CA352740192

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064188C>G (hg19) ; chr3:g.49026755C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026755C>G , CM000665.2:g.49026755C>G	GRCh38
NC_000003.11:g.49064188C>G , CM000665.1:g.49064188C>G	GRCh37
NC_000003.10:g.49039192C>G	NCBI36
NG_012091.1:g.7688G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2791G>C	ENSP00000515567.1:p.Gly931Arg
ENST00000703937.1:c.*1852G>C	ENSP00000515568.1:n.*1852G>C
ENST00000326739.9:c.751G>C MANE Select	ENSP00000321584.4:p.Gly251Arg
ENST00000429182.6:c.751G>C	ENSP00000393525.2:p.Gly251Arg
ENST00000442157.2:c.676G>C	ENSP00000403502.2:p.Gly226Arg
ENST00000462980.2:n.1266G>C
ENST00000472328.2:n.817G>C
ENST00000491610.2:n.711G>C
ENST00000676607.1:n.1047G>C
ENST00000676627.1:n.1481G>C
ENST00000676708.1:n.2031G>C
ENST00000676864.1:n.1900G>C
ENST00000677010.1:c.787G>C	ENSP00000503089.1:p.Gly263Arg
ENST00000677108.1:n.2657G>C
ENST00000677168.1:n.1223G>C
ENST00000677185.1:n.1314G>C
ENST00000677205.1:n.1535G>C
ENST00000677344.1:n.2025G>C
ENST00000677480.1:c.*428G>C	ENSP00000504378.1:n.*428G>C
ENST00000677519.1:n.1461G>C
ENST00000677593.1:n.1307G>C
ENST00000677740.1:n.2256G>C
ENST00000677991.1:n.1924G>C
ENST00000678001.1:n.1244G>C
ENST00000678085.1:n.1307G>C
ENST00000678177.1:n.2600G>C
ENST00000678603.1:n.1829G>C
ENST00000678724.1:c.676G>C	ENSP00000503874.1:p.Gly226Arg
ENST00000678920.1:n.909G>C
ENST00000679019.1:n.1521G>C
ENST00000679117.1:c.*566G>C	ENSP00000503240.1:n.*566G>C
ENST00000679339.1:n.1592G>C
ENST00000326739.8:c.751G>C	ENSP00000321584.4:p.Gly251Arg
ENST00000429182.5:c.545G>C
ENST00000442157.1:c.676G>C	ENSP00000403502.1:p.Gly226Arg
ENST00000462980.1:n.653G>C
ENST00000491610.1:n.711G>C
NM_000884.2:c.751G>C	NP_000875.2:p.Gly251Arg
XM_006713128.2:c.961G>C	XP_006713191.1:p.Gly321Arg
XM_006713128.3:c.961G>C	XP_006713191.1:p.Gly321Arg
XM_017006349.1:c.886G>C	XP_016861838.1:p.Gly296Arg
XM_017006350.1:c.886G>C	XP_016861839.1:p.Gly296Arg
NM_000884.3:c.751G>C MANE Select	NP_000875.2:p.Gly251Arg