Canonical Allele Identifier: CA452441120

Gene: CITED2

Linked Data

• MyVariant Identifiers: chr6:g.139694302C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373165C>A , CM000668.2:g.139373165C>A	GRCh38
NC_000006.11:g.139694302C>A , CM000668.1:g.139694302C>A	GRCh37
NC_000006.10:g.139735995C>A	NCBI36
NG_016169.1:g.6484G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367651.4:c.780G>T MANE Select	ENSP00000356623.2:p.Val260=
ENST00000367651.3:c.780G>T	ENSP00000356623.2:p.Val260=
ENST00000536159.2:c.780G>T	ENSP00000442831.1:p.Val260=
ENST00000537332.2:c.795G>T	ENSP00000444198.2:p.Val265=
ENST00000618718.1:c.609G>T	ENSP00000479918.1:p.Val203=
NM_001168388.2:c.780G>T	NP_001161860.1:p.Val260=
NM_001168389.2:c.795G>T	NP_001161861.2:p.Val265=
NM_006079.4:c.780G>T	NP_006070.2:p.Val260=
NM_006079.5:c.780G>T MANE Select	NP_006070.2:p.Val260=
NM_001168388.3:c.780G>T	NP_001161860.1:p.Val260=
NM_001168389.3:c.795G>T	NP_001161861.2:p.Val265=