Canonical Allele Identifier: CA433629365

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064034G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026601G>C , CM000665.2:g.49026601G>C	GRCh38
NC_000003.11:g.49064034G>C , CM000665.1:g.49064034G>C	GRCh37
NC_000003.10:g.49039038G>C	NCBI36
NG_012091.1:g.7842C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2868C>G	ENSP00000515567.1:p.Ser956=
ENST00000703937.1:c.*1929C>G	ENSP00000515568.1:n.*1929C>G
ENST00000326739.9:c.828C>G MANE Select	ENSP00000321584.4:p.Ser276=
ENST00000429182.6:c.828C>G	ENSP00000393525.2:p.Ser276=
ENST00000442157.2:c.753C>G	ENSP00000403502.2:p.Ser251=
ENST00000462980.2:n.1343C>G
ENST00000472328.2:n.894C>G
ENST00000491610.2:n.788C>G
ENST00000676607.1:n.1124C>G
ENST00000676627.1:n.1558C>G
ENST00000676708.1:n.2108C>G
ENST00000676864.1:n.1977C>G
ENST00000677010.1:c.856-4C>G	ENSP00000503089.1:n.856-4C>G
ENST00000677108.1:n.2811C>G
ENST00000677168.1:n.1300C>G
ENST00000677185.1:n.1391C>G
ENST00000677205.1:n.1612C>G
ENST00000677344.1:n.2102C>G
ENST00000677480.1:c.*505C>G	ENSP00000504378.1:n.*505C>G
ENST00000677519.1:n.1538C>G
ENST00000677593.1:n.1384C>G
ENST00000677740.1:n.2333C>G
ENST00000677991.1:n.2001C>G
ENST00000678001.1:n.1321C>G
ENST00000678085.1:n.1461C>G
ENST00000678177.1:n.2754C>G
ENST00000678603.1:n.1906C>G
ENST00000678724.1:c.753C>G	ENSP00000503874.1:p.Ser251=
ENST00000678920.1:n.986C>G
ENST00000679019.1:n.1675C>G
ENST00000679117.1:c.*643C>G	ENSP00000503240.1:n.*643C>G
ENST00000679339.1:n.1669C>G
ENST00000326739.8:c.828C>G	ENSP00000321584.4:p.Ser276=
ENST00000429182.5:c.622C>G
ENST00000442157.1:c.753C>G	ENSP00000403502.1:p.Ser251=
ENST00000462980.1:n.730C>G
ENST00000491610.1:n.788C>G
NM_000884.2:c.828C>G	NP_000875.2:p.Ser276=
XM_006713128.2:c.1038C>G	XP_006713191.1:p.Ser346=
XM_006713128.3:c.1038C>G	XP_006713191.1:p.Ser346=
XM_017006349.1:c.963C>G	XP_016861838.1:p.Ser321=
XM_017006350.1:c.963C>G	XP_016861839.1:p.Ser321=
NM_000884.3:c.828C>G MANE Select	NP_000875.2:p.Ser276=