Canonical Allele Identifier: CA452441497

Gene: CITED2

Linked Data

• MyVariant Identifiers: chr6:g.139694449T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373312T>G , CM000668.2:g.139373312T>G	GRCh38
NC_000006.11:g.139694449T>G , CM000668.1:g.139694449T>G	GRCh37
NC_000006.10:g.139736142T>G	NCBI36
NG_016169.1:g.6337A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.633A>C MANE Select	ENSP00000356623.2:p.Ala211=
ENST00000367651.3:c.633A>C	ENSP00000356623.2:p.Ala211=
ENST00000536159.2:c.633A>C	ENSP00000442831.1:p.Ala211=
ENST00000537332.2:c.648A>C	ENSP00000444198.2:p.Ala216=
ENST00000618718.1:c.477-15A>C	ENSP00000479918.1:n.477-15A>C
NM_001168388.2:c.633A>C	NP_001161860.1:p.Ala211=
NM_001168389.2:c.648A>C	NP_001161861.2:p.Ala216=
NM_006079.4:c.633A>C	NP_006070.2:p.Ala211=
NM_006079.5:c.633A>C MANE Select	NP_006070.2:p.Ala211=
NM_001168388.3:c.633A>C	NP_001161860.1:p.Ala211=
NM_001168389.3:c.648A>C	NP_001161861.2:p.Ala216=