Canonical Allele Identifier: CA2680562491
Gene: CITED2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.139373022C>T , CM000668.2:g.139373022C>T GRCh38
NC_000006.11:g.139694159C>T , CM000668.1:g.139694159C>T GRCh37
NC_000006.10:g.139735852C>T NCBI36
NG_016169.1:g.6627G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367651.4:c.*110G>A MANE Select ENSP00000356623.2:n.*110G>A
ENST00000367651.3:c.*110G>A ENSP00000356623.2:n.*110G>A
ENST00000536159.2:c.*110G>A ENSP00000442831.1:n.*110G>A
ENST00000537332.2:c.*110G>A ENSP00000444198.2:n.*110G>A
NM_001168388.2:c.*110G>A NP_001161860.1:n.*110G>A
NM_001168389.2:c.*110G>A NP_001161861.2:n.*110G>A
NM_006079.4:c.*110G>A NP_006070.2:n.*110G>A
NM_006079.5:c.*110G>A MANE Select NP_006070.2:n.*110G>A
NM_001168388.3:c.*110G>A NP_001161860.1:n.*110G>A
NM_001168389.3:c.*110G>A NP_001161861.2:n.*110G>A