Canonical Allele Identifier: CA352740574

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064240G>C (hg19) ; chr3:g.49026807G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026807G>C , CM000665.2:g.49026807G>C	GRCh38
NC_000003.11:g.49064240G>C , CM000665.1:g.49064240G>C	GRCh37
NC_000003.10:g.49039244G>C	NCBI36
NG_012091.1:g.7636C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2739C>G	ENSP00000515567.1:p.Tyr913Ter
ENST00000703937.1:c.*1800C>G	ENSP00000515568.1:n.*1800C>G
ENST00000326739.9:c.699C>G MANE Select	ENSP00000321584.4:p.Tyr233Ter
ENST00000429182.6:c.699C>G	ENSP00000393525.2:p.Tyr233Ter
ENST00000442157.2:c.624C>G	ENSP00000403502.2:p.Tyr208Ter
ENST00000462980.2:n.1214C>G
ENST00000472328.2:n.765C>G
ENST00000491610.2:n.659C>G
ENST00000676607.1:n.995C>G
ENST00000676627.1:n.1429C>G
ENST00000676708.1:n.1979C>G
ENST00000676864.1:n.1848C>G
ENST00000677010.1:c.735C>G	ENSP00000503089.1:p.Tyr245Ter
ENST00000677108.1:n.2605C>G
ENST00000677168.1:n.1171C>G
ENST00000677185.1:n.1262C>G
ENST00000677205.1:n.1483C>G
ENST00000677344.1:n.1973C>G
ENST00000677480.1:c.*376C>G	ENSP00000504378.1:n.*376C>G
ENST00000677519.1:n.1409C>G
ENST00000677593.1:n.1255C>G
ENST00000677740.1:n.2204C>G
ENST00000677991.1:n.1872C>G
ENST00000678001.1:n.1192C>G
ENST00000678085.1:n.1255C>G
ENST00000678177.1:n.2548C>G
ENST00000678603.1:n.1777C>G
ENST00000678724.1:c.624C>G	ENSP00000503874.1:p.Tyr208Ter
ENST00000678920.1:n.857C>G
ENST00000679019.1:n.1469C>G
ENST00000679117.1:c.*514C>G	ENSP00000503240.1:n.*514C>G
ENST00000679339.1:n.1540C>G
ENST00000326739.8:c.699C>G	ENSP00000321584.4:p.Tyr233Ter
ENST00000429182.5:c.493C>G
ENST00000442157.1:c.624C>G	ENSP00000403502.1:p.Tyr208Ter
ENST00000462980.1:n.601C>G
ENST00000491610.1:n.659C>G
NM_000884.2:c.699C>G	NP_000875.2:p.Tyr233Ter
XM_006713128.2:c.909C>G	XP_006713191.1:p.Tyr303Ter
XM_006713128.3:c.909C>G	XP_006713191.1:p.Tyr303Ter
XM_017006349.1:c.834C>G	XP_016861838.1:p.Tyr278Ter
XM_017006350.1:c.834C>G	XP_016861839.1:p.Tyr278Ter
NM_000884.3:c.699C>G MANE Select	NP_000875.2:p.Tyr233Ter