Canonical Allele Identifier: CA365876175

Gene: CITED2

Linked Data

• ClinVar Variation Id: 3064915
• ClinVar RCV Id: RCV003989992
• MyVariant Identifiers: chr6:g.139694328C>A (hg19) ; chr6:g.139373191C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373191C>A , CM000668.2:g.139373191C>A	GRCh38
NC_000006.11:g.139694328C>A , CM000668.1:g.139694328C>A	GRCh37
NC_000006.10:g.139736021C>A	NCBI36
NG_016169.1:g.6458G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.754G>T MANE Select	ENSP00000356623.2:p.Glu252Ter
ENST00000367651.3:c.754G>T	ENSP00000356623.2:p.Glu252Ter
ENST00000536159.2:c.754G>T	ENSP00000442831.1:p.Glu252Ter
ENST00000537332.2:c.769G>T	ENSP00000444198.2:p.Glu257Ter
ENST00000618718.1:c.583G>T	ENSP00000479918.1:p.Glu195Ter
NM_001168388.2:c.754G>T	NP_001161860.1:p.Glu252Ter
NM_001168389.2:c.769G>T	NP_001161861.2:p.Glu257Ter
NM_006079.4:c.754G>T	NP_006070.2:p.Glu252Ter
NM_006079.5:c.754G>T MANE Select	NP_006070.2:p.Glu252Ter
NM_001168388.3:c.754G>T	NP_001161860.1:p.Glu252Ter
NM_001168389.3:c.769G>T	NP_001161861.2:p.Glu257Ter