Canonical Allele Identifier: CA1667372102
Gene: CITED2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.139372928A= , CM000668.2:g.139372928A= GRCh38
NC_000006.11:g.139694065A= , CM000668.1:g.139694065A= GRCh37
NC_000006.10:g.139735758A= NCBI36
NG_016169.1:g.6721T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367651.4:c.*204T= MANE Select ENSP00000356623.2:n.*204T=
ENST00000367651.3:c.*204T= ENSP00000356623.2:n.*204T=
ENST00000536159.2:c.*204T= ENSP00000442831.1:n.*204T=
ENST00000537332.2:c.*204T= ENSP00000444198.2:n.*204T=
NM_001168388.2:c.*204T= NP_001161860.1:n.*204T=
NM_001168389.2:c.*204T= NP_001161861.2:n.*204T=
NM_006079.4:c.*204T= NP_006070.2:n.*204T=
NM_006079.5:c.*204T= MANE Select NP_006070.2:n.*204T=
NM_001168388.3:c.*204T= NP_001161860.1:n.*204T=
NM_001168389.3:c.*204T= NP_001161861.2:n.*204T=
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