Canonical Allele Identifier: CA365876813
Gene: CITED2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.139373431C>T , CM000668.2:g.139373431C>T GRCh38
NC_000006.11:g.139694568C>T , CM000668.1:g.139694568C>T GRCh37
NC_000006.10:g.139736261C>T NCBI36
NG_016169.1:g.6218G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367651.4:c.514G>A MANE Select ENSP00000356623.2:p.Gly172Ser
ENST00000367651.3:c.514G>A ENSP00000356623.2:p.Gly172Ser
ENST00000536159.2:c.514G>A ENSP00000442831.1:p.Gly172Ser
ENST00000537332.2:c.529G>A ENSP00000444198.2:p.Gly177Ser
ENST00000618718.1:c.476+38G>A ENSP00000479918.1:n.476+38G>A
NM_001168388.2:c.514G>A NP_001161860.1:p.Gly172Ser
NM_001168389.2:c.529G>A NP_001161861.2:p.Gly177Ser
NM_006079.4:c.514G>A NP_006070.2:p.Gly172Ser
NM_006079.5:c.514G>A MANE Select NP_006070.2:p.Gly172Ser
NM_001168388.3:c.514G>A NP_001161860.1:p.Gly172Ser
NM_001168389.3:c.529G>A NP_001161861.2:p.Gly177Ser