Canonical Allele Identifier: CA352740581

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064241T>C (hg19) ; chr3:g.49026808T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026808T>C , CM000665.2:g.49026808T>C	GRCh38
NC_000003.11:g.49064241T>C , CM000665.1:g.49064241T>C	GRCh37
NC_000003.10:g.49039245T>C	NCBI36
NG_012091.1:g.7635A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2738A>G	ENSP00000515567.1:p.Tyr913Cys
ENST00000703937.1:c.*1799A>G	ENSP00000515568.1:n.*1799A>G
ENST00000326739.9:c.698A>G MANE Select	ENSP00000321584.4:p.Tyr233Cys
ENST00000429182.6:c.698A>G	ENSP00000393525.2:p.Tyr233Cys
ENST00000442157.2:c.623A>G	ENSP00000403502.2:p.Tyr208Cys
ENST00000462980.2:n.1213A>G
ENST00000472328.2:n.764A>G
ENST00000491610.2:n.658A>G
ENST00000676607.1:n.994A>G
ENST00000676627.1:n.1428A>G
ENST00000676708.1:n.1978A>G
ENST00000676864.1:n.1847A>G
ENST00000677010.1:c.734A>G	ENSP00000503089.1:p.Tyr245Cys
ENST00000677108.1:n.2604A>G
ENST00000677168.1:n.1170A>G
ENST00000677185.1:n.1261A>G
ENST00000677205.1:n.1482A>G
ENST00000677344.1:n.1972A>G
ENST00000677480.1:c.*375A>G	ENSP00000504378.1:n.*375A>G
ENST00000677519.1:n.1408A>G
ENST00000677593.1:n.1254A>G
ENST00000677740.1:n.2203A>G
ENST00000677991.1:n.1871A>G
ENST00000678001.1:n.1191A>G
ENST00000678085.1:n.1254A>G
ENST00000678177.1:n.2547A>G
ENST00000678603.1:n.1776A>G
ENST00000678724.1:c.623A>G	ENSP00000503874.1:p.Tyr208Cys
ENST00000678920.1:n.856A>G
ENST00000679019.1:n.1468A>G
ENST00000679117.1:c.*513A>G	ENSP00000503240.1:n.*513A>G
ENST00000679339.1:n.1539A>G
ENST00000326739.8:c.698A>G	ENSP00000321584.4:p.Tyr233Cys
ENST00000429182.5:c.492A>G
ENST00000442157.1:c.623A>G	ENSP00000403502.1:p.Tyr208Cys
ENST00000462980.1:n.600A>G
ENST00000491610.1:n.658A>G
NM_000884.2:c.698A>G	NP_000875.2:p.Tyr233Cys
XM_006713128.2:c.908A>G	XP_006713191.1:p.Tyr303Cys
XM_006713128.3:c.908A>G	XP_006713191.1:p.Tyr303Cys
XM_017006349.1:c.833A>G	XP_016861838.1:p.Tyr278Cys
XM_017006350.1:c.833A>G	XP_016861839.1:p.Tyr278Cys
NM_000884.3:c.698A>G MANE Select	NP_000875.2:p.Tyr233Cys