Canonical Allele Identifier: CA352740165

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064185T>G (hg19) ; chr3:g.49026752T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026752T>G , CM000665.2:g.49026752T>G	GRCh38
NC_000003.11:g.49064185T>G , CM000665.1:g.49064185T>G	GRCh37
NC_000003.10:g.49039189T>G	NCBI36
NG_012091.1:g.7691A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2794A>C	ENSP00000515567.1:p.Thr932Pro
ENST00000703937.1:c.*1855A>C	ENSP00000515568.1:n.*1855A>C
ENST00000326739.9:c.754A>C MANE Select	ENSP00000321584.4:p.Thr252Pro
ENST00000429182.6:c.754A>C	ENSP00000393525.2:p.Thr252Pro
ENST00000442157.2:c.679A>C	ENSP00000403502.2:p.Thr227Pro
ENST00000462980.2:n.1269A>C
ENST00000472328.2:n.820A>C
ENST00000491610.2:n.714A>C
ENST00000676607.1:n.1050A>C
ENST00000676627.1:n.1484A>C
ENST00000676708.1:n.2034A>C
ENST00000676864.1:n.1903A>C
ENST00000677010.1:c.790A>C	ENSP00000503089.1:p.Thr264Pro
ENST00000677108.1:n.2660A>C
ENST00000677168.1:n.1226A>C
ENST00000677185.1:n.1317A>C
ENST00000677205.1:n.1538A>C
ENST00000677344.1:n.2028A>C
ENST00000677480.1:c.*431A>C	ENSP00000504378.1:n.*431A>C
ENST00000677519.1:n.1464A>C
ENST00000677593.1:n.1310A>C
ENST00000677740.1:n.2259A>C
ENST00000677991.1:n.1927A>C
ENST00000678001.1:n.1247A>C
ENST00000678085.1:n.1310A>C
ENST00000678177.1:n.2603A>C
ENST00000678603.1:n.1832A>C
ENST00000678724.1:c.679A>C	ENSP00000503874.1:p.Thr227Pro
ENST00000678920.1:n.912A>C
ENST00000679019.1:n.1524A>C
ENST00000679117.1:c.*569A>C	ENSP00000503240.1:n.*569A>C
ENST00000679339.1:n.1595A>C
ENST00000326739.8:c.754A>C	ENSP00000321584.4:p.Thr252Pro
ENST00000429182.5:c.548A>C
ENST00000442157.1:c.679A>C	ENSP00000403502.1:p.Thr227Pro
ENST00000462980.1:n.656A>C
ENST00000491610.1:n.714A>C
NM_000884.2:c.754A>C	NP_000875.2:p.Thr252Pro
XM_006713128.2:c.964A>C	XP_006713191.1:p.Thr322Pro
XM_006713128.3:c.964A>C	XP_006713191.1:p.Thr322Pro
XM_017006349.1:c.889A>C	XP_016861838.1:p.Thr297Pro
XM_017006350.1:c.889A>C	XP_016861839.1:p.Thr297Pro
NM_000884.3:c.754A>C MANE Select	NP_000875.2:p.Thr252Pro