Canonical Allele Identifier: CA452441528

Gene: CITED2

Linked Data

• MyVariant Identifiers: chr6:g.139694467C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373330C>G , CM000668.2:g.139373330C>G	GRCh38
NC_000006.11:g.139694467C>G , CM000668.1:g.139694467C>G	GRCh37
NC_000006.10:g.139736160C>G	NCBI36
NG_016169.1:g.6319G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.615G>C MANE Select	ENSP00000356623.2:p.Val205=
ENST00000367651.3:c.615G>C	ENSP00000356623.2:p.Val205=
ENST00000536159.2:c.615G>C	ENSP00000442831.1:p.Val205=
ENST00000537332.2:c.630G>C	ENSP00000444198.2:p.Val210=
ENST00000618718.1:c.477-33G>C	ENSP00000479918.1:n.477-33G>C
NM_001168388.2:c.615G>C	NP_001161860.1:p.Val205=
NM_001168389.2:c.630G>C	NP_001161861.2:p.Val210=
NM_006079.4:c.615G>C	NP_006070.2:p.Val205=
NM_006079.5:c.615G>C MANE Select	NP_006070.2:p.Val205=
NM_001168388.3:c.615G>C	NP_001161860.1:p.Val205=
NM_001168389.3:c.630G>C	NP_001161861.2:p.Val210=