Canonical Allele Identifier: CA2680562518
Gene: CITED2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.139373059T>A , CM000668.2:g.139373059T>A GRCh38
NC_000006.11:g.139694196T>A , CM000668.1:g.139694196T>A GRCh37
NC_000006.10:g.139735889T>A NCBI36
NG_016169.1:g.6590A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367651.4:c.*73A>T MANE Select ENSP00000356623.2:n.*73A>T
ENST00000367651.3:c.*73A>T ENSP00000356623.2:n.*73A>T
ENST00000536159.2:c.*73A>T ENSP00000442831.1:n.*73A>T
ENST00000537332.2:c.*73A>T ENSP00000444198.2:n.*73A>T
NM_001168388.2:c.*73A>T NP_001161860.1:n.*73A>T
NM_001168389.2:c.*73A>T NP_001161861.2:n.*73A>T
NM_006079.4:c.*73A>T NP_006070.2:n.*73A>T
NM_006079.5:c.*73A>T MANE Select NP_006070.2:n.*73A>T
NM_001168388.3:c.*73A>T NP_001161860.1:n.*73A>T
NM_001168389.3:c.*73A>T NP_001161861.2:n.*73A>T