Canonical Allele Identifier: CA365876779
Gene: CITED2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.139373415C>T , CM000668.2:g.139373415C>T GRCh38
NC_000006.11:g.139694552C>T , CM000668.1:g.139694552C>T GRCh37
NC_000006.10:g.139736245C>T NCBI36
NG_016169.1:g.6234G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367651.4:c.530G>A MANE Select ENSP00000356623.2:p.Gly177Asp
ENST00000367651.3:c.530G>A ENSP00000356623.2:p.Gly177Asp
ENST00000536159.2:c.530G>A ENSP00000442831.1:p.Gly177Asp
ENST00000537332.2:c.545G>A ENSP00000444198.2:p.Gly182Asp
ENST00000618718.1:c.476+54G>A ENSP00000479918.1:n.476+54G>A
NM_001168388.2:c.530G>A NP_001161860.1:p.Gly177Asp
NM_001168389.2:c.545G>A NP_001161861.2:p.Gly182Asp
NM_006079.4:c.530G>A NP_006070.2:p.Gly177Asp
NM_006079.5:c.530G>A MANE Select NP_006070.2:p.Gly177Asp
NM_001168388.3:c.530G>A NP_001161860.1:p.Gly177Asp
NM_001168389.3:c.545G>A NP_001161861.2:p.Gly182Asp