Canonical Allele Identifier: CA148813767
Gene: CITED2 HGNC NCBI

Linked Data

dbSNP Id: rs562937099

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.139373002T>A , CM000668.2:g.139373002T>A GRCh38
NC_000006.11:g.139694139T>A , CM000668.1:g.139694139T>A GRCh37
NC_000006.10:g.139735832T>A NCBI36
NG_016169.1:g.6647A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367651.4:c.*130A>T MANE Select ENSP00000356623.2:n.*130A>T
ENST00000367651.3:c.*130A>T ENSP00000356623.2:n.*130A>T
ENST00000536159.2:c.*130A>T ENSP00000442831.1:n.*130A>T
ENST00000537332.2:c.*130A>T ENSP00000444198.2:n.*130A>T
NM_001168388.2:c.*130A>T NP_001161860.1:n.*130A>T
NM_001168389.2:c.*130A>T NP_001161861.2:n.*130A>T
NM_006079.4:c.*130A>T NP_006070.2:n.*130A>T
NM_006079.5:c.*130A>T MANE Select NP_006070.2:n.*130A>T
NM_001168388.3:c.*130A>T NP_001161860.1:n.*130A>T
NM_001168389.3:c.*130A>T NP_001161861.2:n.*130A>T