Canonical Allele Identifier: CA352741694

Gene: IMPDH2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2633A>G	ENSP00000515567.1:p.Asn878Ser
ENST00000703937.1:c.*1694A>G	ENSP00000515568.1:n.*1694A>G
ENST00000326739.9:c.593A>G MANE Select	ENSP00000321584.4:p.Asn198Ser
ENST00000429182.6:c.593A>G	ENSP00000393525.2:p.Asn198Ser
ENST00000442157.2:c.518A>G	ENSP00000403502.2:p.Asn173Ser
ENST00000462980.2:n.1108A>G
ENST00000472328.2:n.659A>G
ENST00000491610.2:n.480A>G
ENST00000676607.1:n.889A>G
ENST00000676627.1:n.1323A>G
ENST00000676708.1:n.1800A>G
ENST00000676864.1:n.1669A>G
ENST00000677010.1:c.629A>G	ENSP00000503089.1:p.Asn210Ser
ENST00000677108.1:n.2426A>G
ENST00000677168.1:n.1065A>G
ENST00000677185.1:n.1083A>G
ENST00000677205.1:n.1304A>G
ENST00000677344.1:n.1794A>G
ENST00000677480.1:c.*270A>G	ENSP00000504378.1:n.*270A>G
ENST00000677519.1:n.1303A>G
ENST00000677593.1:n.1076A>G
ENST00000677740.1:n.2025A>G
ENST00000677991.1:n.1766A>G
ENST00000678001.1:n.1086A>G
ENST00000678085.1:n.1076A>G
ENST00000678177.1:n.2369A>G
ENST00000678603.1:n.1671A>G
ENST00000678724.1:c.518A>G	ENSP00000503874.1:p.Asn173Ser
ENST00000678920.1:n.751A>G
ENST00000679019.1:n.1290A>G
ENST00000679117.1:c.*408A>G	ENSP00000503240.1:n.*408A>G
ENST00000679339.1:n.1361A>G
ENST00000326739.8:c.593A>G	ENSP00000321584.4:p.Asn198Ser
ENST00000429182.5:c.387A>G
ENST00000442157.1:c.518A>G	ENSP00000403502.1:p.Asn173Ser
ENST00000462980.1:n.495A>G
ENST00000491610.1:n.480A>G
NM_000884.2:c.593A>G	NP_000875.2:p.Asn198Ser
XM_006713128.2:c.803A>G	XP_006713191.1:p.Asn268Ser
XM_006713128.3:c.803A>G	XP_006713191.1:p.Asn268Ser
XM_017006349.1:c.728A>G	XP_016861838.1:p.Asn243Ser
XM_017006350.1:c.728A>G	XP_016861839.1:p.Asn243Ser
NM_000884.3:c.593A>G MANE Select	NP_000875.2:p.Asn198Ser