Canonical Allele Identifier: CA365876514

Gene: CITED2

Linked Data

• MyVariant Identifiers: chr6:g.139694420T>A (hg19) ; chr6:g.139373283T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373283T>A , CM000668.2:g.139373283T>A	GRCh38
NC_000006.11:g.139694420T>A , CM000668.1:g.139694420T>A	GRCh37
NC_000006.10:g.139736113T>A	NCBI36
NG_016169.1:g.6366A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.662A>T MANE Select	ENSP00000356623.2:p.Asp221Val
ENST00000367651.3:c.662A>T	ENSP00000356623.2:p.Asp221Val
ENST00000536159.2:c.662A>T	ENSP00000442831.1:p.Asp221Val
ENST00000537332.2:c.677A>T	ENSP00000444198.2:p.Asp226Val
ENST00000618718.1:c.491A>T	ENSP00000479918.1:p.Asp164Val
NM_001168388.2:c.662A>T	NP_001161860.1:p.Asp221Val
NM_001168389.2:c.677A>T	NP_001161861.2:p.Asp226Val
NM_006079.4:c.662A>T	NP_006070.2:p.Asp221Val
NM_006079.5:c.662A>T MANE Select	NP_006070.2:p.Asp221Val
NM_001168388.3:c.662A>T	NP_001161860.1:p.Asp221Val
NM_001168389.3:c.677A>T	NP_001161861.2:p.Asp226Val