Canonical Allele Identifier: CA433629660

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064273A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026840A>G , CM000665.2:g.49026840A>G	GRCh38
NC_000003.11:g.49064273A>G , CM000665.1:g.49064273A>G	GRCh37
NC_000003.10:g.49039277A>G	NCBI36
NG_012091.1:g.7603T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2706T>C	ENSP00000515567.1:p.Ile902=
ENST00000703937.1:c.*1767T>C	ENSP00000515568.1:n.*1767T>C
ENST00000326739.9:c.666T>C MANE Select	ENSP00000321584.4:p.Ile222=
ENST00000429182.6:c.666T>C	ENSP00000393525.2:p.Ile222=
ENST00000442157.2:c.591T>C	ENSP00000403502.2:p.Ile197=
ENST00000462980.2:n.1181T>C
ENST00000472328.2:n.732T>C
ENST00000491610.2:n.626T>C
ENST00000676607.1:n.962T>C
ENST00000676627.1:n.1396T>C
ENST00000676708.1:n.1946T>C
ENST00000676864.1:n.1815T>C
ENST00000677010.1:c.702T>C	ENSP00000503089.1:p.Ile234=
ENST00000677108.1:n.2572T>C
ENST00000677168.1:n.1138T>C
ENST00000677185.1:n.1229T>C
ENST00000677205.1:n.1450T>C
ENST00000677344.1:n.1940T>C
ENST00000677480.1:c.*343T>C	ENSP00000504378.1:n.*343T>C
ENST00000677519.1:n.1376T>C
ENST00000677593.1:n.1222T>C
ENST00000677740.1:n.2171T>C
ENST00000677991.1:n.1839T>C
ENST00000678001.1:n.1159T>C
ENST00000678085.1:n.1222T>C
ENST00000678177.1:n.2515T>C
ENST00000678603.1:n.1744T>C
ENST00000678724.1:c.591T>C	ENSP00000503874.1:p.Ile197=
ENST00000678920.1:n.824T>C
ENST00000679019.1:n.1436T>C
ENST00000679117.1:c.*481T>C	ENSP00000503240.1:n.*481T>C
ENST00000679339.1:n.1507T>C
ENST00000326739.8:c.666T>C	ENSP00000321584.4:p.Ile222=
ENST00000429182.5:c.460T>C
ENST00000442157.1:c.591T>C	ENSP00000403502.1:p.Ile197=
ENST00000462980.1:n.568T>C
ENST00000491610.1:n.626T>C
NM_000884.2:c.666T>C	NP_000875.2:p.Ile222=
XM_006713128.2:c.876T>C	XP_006713191.1:p.Ile292=
XM_006713128.3:c.876T>C	XP_006713191.1:p.Ile292=
XM_017006349.1:c.801T>C	XP_016861838.1:p.Ile267=
XM_017006350.1:c.801T>C	XP_016861839.1:p.Ile267=
NM_000884.3:c.666T>C MANE Select	NP_000875.2:p.Ile222=