Canonical Allele Identifier: CA352739787

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064119C>A (hg19) ; chr3:g.49026686C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026686C>A , CM000665.2:g.49026686C>A	GRCh38
NC_000003.11:g.49064119C>A , CM000665.1:g.49064119C>A	GRCh37
NC_000003.10:g.49039123C>A	NCBI36
NG_012091.1:g.7757G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000703936.1:c.2859+1G>T	ENSP00000515567.1:n.2859+1G>T
ENST00000703937.1:c.*1920+1G>T	ENSP00000515568.1:n.*1920+1G>T
ENST00000326739.9:c.819+1G>T MANE Select	ENSP00000321584.4:n.819+1G>T
ENST00000429182.6:c.819+1G>T	ENSP00000393525.2:n.819+1G>T
ENST00000442157.2:c.744+1G>T	ENSP00000403502.2:n.744+1G>T
ENST00000462980.2:n.1334+1G>T
ENST00000472328.2:n.885+1G>T
ENST00000491610.2:n.779+1G>T
ENST00000676607.1:n.1115+1G>T
ENST00000676627.1:n.1549+1G>T
ENST00000676708.1:n.2099+1G>T
ENST00000676864.1:n.1968+1G>T
ENST00000677010.1:c.855+1G>T	ENSP00000503089.1:n.855+1G>T
ENST00000677108.1:n.2726G>T
ENST00000677168.1:n.1291+1G>T
ENST00000677185.1:n.1382+1G>T
ENST00000677205.1:n.1603+1G>T
ENST00000677344.1:n.2093+1G>T
ENST00000677480.1:c.*496+1G>T	ENSP00000504378.1:n.*496+1G>T
ENST00000677519.1:n.1529+1G>T
ENST00000677593.1:n.1375+1G>T
ENST00000677740.1:n.2324+1G>T
ENST00000677991.1:n.1992+1G>T
ENST00000678001.1:n.1312+1G>T
ENST00000678085.1:n.1376G>T
ENST00000678177.1:n.2669G>T
ENST00000678603.1:n.1897+1G>T
ENST00000678724.1:c.744+1G>T	ENSP00000503874.1:n.744+1G>T
ENST00000678920.1:n.977+1G>T
ENST00000679019.1:n.1590G>T
ENST00000679117.1:c.*634+1G>T	ENSP00000503240.1:n.*634+1G>T
ENST00000679339.1:n.1660+1G>T
ENST00000326739.8:c.819+1G>T	ENSP00000321584.4:n.819+1G>T
ENST00000429182.5:c.613+1G>T
ENST00000442157.1:c.744+1G>T	ENSP00000403502.1:n.744+1G>T
ENST00000462980.1:n.721+1G>T
ENST00000491610.1:n.779+1G>T
NM_000884.2:c.819+1G>T	NP_000875.2:n.819+1G>T
XM_006713128.2:c.1029+1G>T	XP_006713191.1:n.1029+1G>T
XM_006713128.3:c.1029+1G>T	XP_006713191.1:n.1029+1G>T
XM_017006349.1:c.954+1G>T	XP_016861838.1:n.954+1G>T
XM_017006350.1:c.954+1G>T	XP_016861839.1:n.954+1G>T
NM_000884.3:c.819+1G>T MANE Select	NP_000875.2:n.819+1G>T