Canonical Allele Identifier: CA352739744

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064044T>G (hg19) ; chr3:g.49026611T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026611T>G , CM000665.2:g.49026611T>G	GRCh38
NC_000003.11:g.49064044T>G , CM000665.1:g.49064044T>G	GRCh37
NC_000003.10:g.49039048T>G	NCBI36
NG_012091.1:g.7832A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2860-2A>C	ENSP00000515567.1:n.2860-2A>C
ENST00000703937.1:c.*1921-2A>C	ENSP00000515568.1:n.*1921-2A>C
ENST00000326739.9:c.820-2A>C MANE Select	ENSP00000321584.4:n.820-2A>C
ENST00000429182.6:c.820-2A>C	ENSP00000393525.2:n.820-2A>C
ENST00000442157.2:c.745-2A>C	ENSP00000403502.2:n.745-2A>C
ENST00000462980.2:n.1335-2A>C
ENST00000472328.2:n.886-2A>C
ENST00000491610.2:n.780-2A>C
ENST00000676607.1:n.1116-2A>C
ENST00000676627.1:n.1550-2A>C
ENST00000676708.1:n.2100-2A>C
ENST00000676864.1:n.1969-2A>C
ENST00000677010.1:c.856-14A>C	ENSP00000503089.1:n.856-14A>C
ENST00000677108.1:n.2801A>C
ENST00000677168.1:n.1292-2A>C
ENST00000677185.1:n.1383-2A>C
ENST00000677205.1:n.1604-2A>C
ENST00000677344.1:n.2094-2A>C
ENST00000677480.1:c.*497-2A>C	ENSP00000504378.1:n.*497-2A>C
ENST00000677519.1:n.1530-2A>C
ENST00000677593.1:n.1376-2A>C
ENST00000677740.1:n.2325-2A>C
ENST00000677991.1:n.1993-2A>C
ENST00000678001.1:n.1313-2A>C
ENST00000678085.1:n.1451A>C
ENST00000678177.1:n.2744A>C
ENST00000678603.1:n.1898-2A>C
ENST00000678724.1:c.745-2A>C	ENSP00000503874.1:n.745-2A>C
ENST00000678920.1:n.978-2A>C
ENST00000679019.1:n.1665A>C
ENST00000679117.1:c.*635-2A>C	ENSP00000503240.1:n.*635-2A>C
ENST00000679339.1:n.1661-2A>C
ENST00000326739.8:c.820-2A>C	ENSP00000321584.4:n.820-2A>C
ENST00000429182.5:c.614-2A>C
ENST00000442157.1:c.745-2A>C	ENSP00000403502.1:n.745-2A>C
ENST00000462980.1:n.722-2A>C
ENST00000491610.1:n.780-2A>C
NM_000884.2:c.820-2A>C	NP_000875.2:n.820-2A>C
XM_006713128.2:c.1030-2A>C	XP_006713191.1:n.1030-2A>C
XM_006713128.3:c.1030-2A>C	XP_006713191.1:n.1030-2A>C
XM_017006349.1:c.955-2A>C	XP_016861838.1:n.955-2A>C
XM_017006350.1:c.955-2A>C	XP_016861839.1:n.955-2A>C
NM_000884.3:c.820-2A>C MANE Select	NP_000875.2:n.820-2A>C