Canonical Allele Identifier: CA452441439

Gene: CITED2

Linked Data

• MyVariant Identifiers: chr6:g.139694422A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373285A>C , CM000668.2:g.139373285A>C	GRCh38
NC_000006.11:g.139694422A>C , CM000668.1:g.139694422A>C	GRCh37
NC_000006.10:g.139736115A>C	NCBI36
NG_016169.1:g.6364T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.660T>G MANE Select	ENSP00000356623.2:p.Thr220=
ENST00000367651.3:c.660T>G	ENSP00000356623.2:p.Thr220=
ENST00000536159.2:c.660T>G	ENSP00000442831.1:p.Thr220=
ENST00000537332.2:c.675T>G	ENSP00000444198.2:p.Thr225=
ENST00000618718.1:c.489T>G	ENSP00000479918.1:p.Thr163=
NM_001168388.2:c.660T>G	NP_001161860.1:p.Thr220=
NM_001168389.2:c.675T>G	NP_001161861.2:p.Thr225=
NM_006079.4:c.660T>G	NP_006070.2:p.Thr220=
NM_006079.5:c.660T>G MANE Select	NP_006070.2:p.Thr220=
NM_001168388.3:c.660T>G	NP_001161860.1:p.Thr220=
NM_001168389.3:c.675T>G	NP_001161861.2:p.Thr225=