Canonical Allele Identifier: CA352741677

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064419T>G (hg19) ; chr3:g.49026986T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026986T>G , CM000665.2:g.49026986T>G	GRCh38
NC_000003.11:g.49064419T>G , CM000665.1:g.49064419T>G	GRCh37
NC_000003.10:g.49039423T>G	NCBI36
NG_012091.1:g.7457A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2633A>C	ENSP00000515567.1:p.Asn878Thr
ENST00000703937.1:c.*1694A>C	ENSP00000515568.1:n.*1694A>C
ENST00000326739.9:c.593A>C MANE Select	ENSP00000321584.4:p.Asn198Thr
ENST00000429182.6:c.593A>C	ENSP00000393525.2:p.Asn198Thr
ENST00000442157.2:c.518A>C	ENSP00000403502.2:p.Asn173Thr
ENST00000462980.2:n.1108A>C
ENST00000472328.2:n.659A>C
ENST00000491610.2:n.480A>C
ENST00000676607.1:n.889A>C
ENST00000676627.1:n.1323A>C
ENST00000676708.1:n.1800A>C
ENST00000676864.1:n.1669A>C
ENST00000677010.1:c.629A>C	ENSP00000503089.1:p.Asn210Thr
ENST00000677108.1:n.2426A>C
ENST00000677168.1:n.1065A>C
ENST00000677185.1:n.1083A>C
ENST00000677205.1:n.1304A>C
ENST00000677344.1:n.1794A>C
ENST00000677480.1:c.*270A>C	ENSP00000504378.1:n.*270A>C
ENST00000677519.1:n.1303A>C
ENST00000677593.1:n.1076A>C
ENST00000677740.1:n.2025A>C
ENST00000677991.1:n.1766A>C
ENST00000678001.1:n.1086A>C
ENST00000678085.1:n.1076A>C
ENST00000678177.1:n.2369A>C
ENST00000678603.1:n.1671A>C
ENST00000678724.1:c.518A>C	ENSP00000503874.1:p.Asn173Thr
ENST00000678920.1:n.751A>C
ENST00000679019.1:n.1290A>C
ENST00000679117.1:c.*408A>C	ENSP00000503240.1:n.*408A>C
ENST00000679339.1:n.1361A>C
ENST00000326739.8:c.593A>C	ENSP00000321584.4:p.Asn198Thr
ENST00000429182.5:c.387A>C
ENST00000442157.1:c.518A>C	ENSP00000403502.1:p.Asn173Thr
ENST00000462980.1:n.495A>C
ENST00000491610.1:n.480A>C
NM_000884.2:c.593A>C	NP_000875.2:p.Asn198Thr
XM_006713128.2:c.803A>C	XP_006713191.1:p.Asn268Thr
XM_006713128.3:c.803A>C	XP_006713191.1:p.Asn268Thr
XM_017006349.1:c.728A>C	XP_016861838.1:p.Asn243Thr
XM_017006350.1:c.728A>C	XP_016861839.1:p.Asn243Thr
NM_000884.3:c.593A>C MANE Select	NP_000875.2:p.Asn198Thr