Canonical Allele Identifier: CA352741175

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064307A>C (hg19) ; chr3:g.49026874A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026874A>C , CM000665.2:g.49026874A>C	GRCh38
NC_000003.11:g.49064307A>C , CM000665.1:g.49064307A>C	GRCh37
NC_000003.10:g.49039311A>C	NCBI36
NG_012091.1:g.7569T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2672T>G	ENSP00000515567.1:p.Ile891Ser
ENST00000703937.1:c.*1733T>G	ENSP00000515568.1:n.*1733T>G
ENST00000326739.9:c.632T>G MANE Select	ENSP00000321584.4:p.Ile211Ser
ENST00000429182.6:c.632T>G	ENSP00000393525.2:p.Ile211Ser
ENST00000442157.2:c.557T>G	ENSP00000403502.2:p.Ile186Ser
ENST00000462980.2:n.1147T>G
ENST00000472328.2:n.698T>G
ENST00000491610.2:n.592T>G
ENST00000676607.1:n.928T>G
ENST00000676627.1:n.1362T>G
ENST00000676708.1:n.1912T>G
ENST00000676864.1:n.1781T>G
ENST00000677010.1:c.668T>G	ENSP00000503089.1:p.Ile223Ser
ENST00000677108.1:n.2538T>G
ENST00000677168.1:n.1104T>G
ENST00000677185.1:n.1195T>G
ENST00000677205.1:n.1416T>G
ENST00000677344.1:n.1906T>G
ENST00000677480.1:c.*309T>G	ENSP00000504378.1:n.*309T>G
ENST00000677519.1:n.1342T>G
ENST00000677593.1:n.1188T>G
ENST00000677740.1:n.2137T>G
ENST00000677991.1:n.1805T>G
ENST00000678001.1:n.1125T>G
ENST00000678085.1:n.1188T>G
ENST00000678177.1:n.2481T>G
ENST00000678603.1:n.1710T>G
ENST00000678724.1:c.557T>G	ENSP00000503874.1:p.Ile186Ser
ENST00000678920.1:n.790T>G
ENST00000679019.1:n.1402T>G
ENST00000679117.1:c.*447T>G	ENSP00000503240.1:n.*447T>G
ENST00000679339.1:n.1473T>G
ENST00000326739.8:c.632T>G	ENSP00000321584.4:p.Ile211Ser
ENST00000429182.5:c.426T>G
ENST00000442157.1:c.557T>G	ENSP00000403502.1:p.Ile186Ser
ENST00000462980.1:n.534T>G
ENST00000491610.1:n.592T>G
NM_000884.2:c.632T>G	NP_000875.2:p.Ile211Ser
XM_006713128.2:c.842T>G	XP_006713191.1:p.Ile281Ser
XM_006713128.3:c.842T>G	XP_006713191.1:p.Ile281Ser
XM_017006349.1:c.767T>G	XP_016861838.1:p.Ile256Ser
XM_017006350.1:c.767T>G	XP_016861839.1:p.Ile256Ser
NM_000884.3:c.632T>G MANE Select	NP_000875.2:p.Ile211Ser