Canonical Allele Identifier: CA352739571

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064017A>G (hg19) ; chr3:g.49026584A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026584A>G , CM000665.2:g.49026584A>G	GRCh38
NC_000003.11:g.49064017A>G , CM000665.1:g.49064017A>G	GRCh37
NC_000003.10:g.49039021A>G	NCBI36
NG_012091.1:g.7859T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000703936.1:c.2885T>C	ENSP00000515567.1:p.Phe962Ser
ENST00000703937.1:c.*1946T>C	ENSP00000515568.1:n.*1946T>C
ENST00000326739.9:c.845T>C MANE Select	ENSP00000321584.4:p.Phe282Ser
ENST00000429182.6:c.845T>C	ENSP00000393525.2:p.Phe282Ser
ENST00000442157.2:c.770T>C	ENSP00000403502.2:p.Phe257Ser
ENST00000462980.2:n.1360T>C
ENST00000472328.2:n.911T>C
ENST00000491610.2:n.805T>C
ENST00000676607.1:n.1141T>C
ENST00000676627.1:n.1575T>C
ENST00000676708.1:n.2125T>C
ENST00000676864.1:n.1994T>C
ENST00000677010.1:c.869T>C	ENSP00000503089.1:p.Phe290Ser
ENST00000677108.1:n.2828T>C
ENST00000677168.1:n.1317T>C
ENST00000677185.1:n.1408T>C
ENST00000677205.1:n.1629T>C
ENST00000677344.1:n.2119T>C
ENST00000677480.1:c.*522T>C	ENSP00000504378.1:n.*522T>C
ENST00000677519.1:n.1555T>C
ENST00000677593.1:n.1401T>C
ENST00000677740.1:n.2350T>C
ENST00000677991.1:n.2018T>C
ENST00000678001.1:n.1338T>C
ENST00000678085.1:n.1478T>C
ENST00000678177.1:n.2771T>C
ENST00000678603.1:n.1923T>C
ENST00000678724.1:c.770T>C	ENSP00000503874.1:p.Phe257Ser
ENST00000678920.1:n.1003T>C
ENST00000679019.1:n.1692T>C
ENST00000679117.1:c.*660T>C	ENSP00000503240.1:n.*660T>C
ENST00000679339.1:n.1686T>C
ENST00000326739.8:c.845T>C	ENSP00000321584.4:p.Phe282Ser
ENST00000429182.5:c.639T>C
ENST00000442157.1:c.770T>C	ENSP00000403502.1:p.Phe257Ser
ENST00000462980.1:n.747T>C
ENST00000491610.1:n.805T>C
NM_000884.2:c.845T>C	NP_000875.2:p.Phe282Ser
XM_006713128.2:c.1055T>C	XP_006713191.1:p.Phe352Ser
XM_006713128.3:c.1055T>C	XP_006713191.1:p.Phe352Ser
XM_017006349.1:c.980T>C	XP_016861838.1:p.Phe327Ser
XM_017006350.1:c.980T>C	XP_016861839.1:p.Phe327Ser
NM_000884.3:c.845T>C MANE Select	NP_000875.2:p.Phe282Ser