Canonical Allele Identifier: CA365876829
Gene: CITED2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.139373440C>G , CM000668.2:g.139373440C>G GRCh38
NC_000006.11:g.139694577C>G , CM000668.1:g.139694577C>G GRCh37
NC_000006.10:g.139736270C>G NCBI36
NG_016169.1:g.6209G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367651.4:c.505G>C MANE Select ENSP00000356623.2:p.Gly169Arg
ENST00000367651.3:c.505G>C ENSP00000356623.2:p.Gly169Arg
ENST00000536159.2:c.505G>C ENSP00000442831.1:p.Gly169Arg
ENST00000537332.2:c.520G>C ENSP00000444198.2:p.Gly174Arg
ENST00000618718.1:c.476+29G>C ENSP00000479918.1:n.476+29G>C
NM_001168388.2:c.505G>C NP_001161860.1:p.Gly169Arg
NM_001168389.2:c.520G>C NP_001161861.2:p.Gly174Arg
NM_006079.4:c.505G>C NP_006070.2:p.Gly169Arg
NM_006079.5:c.505G>C MANE Select NP_006070.2:p.Gly169Arg
NM_001168388.3:c.505G>C NP_001161860.1:p.Gly169Arg
NM_001168389.3:c.520G>C NP_001161861.2:p.Gly174Arg