Canonical Allele Identifier: CA1667371958
Gene: CITED2 HGNC NCBI

Linked Data

dbSNP Id: rs1778272129
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.139372703C>G , CM000668.2:g.139372703C>G GRCh38
NC_000006.11:g.139693840C>G , CM000668.1:g.139693840C>G GRCh37
NC_000006.10:g.139735533C>G NCBI36
NG_016169.1:g.6946G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367651.4:c.*429G>C MANE Select ENSP00000356623.2:n.*429G>C
ENST00000367651.3:c.*429G>C ENSP00000356623.2:n.*429G>C
ENST00000536159.2:c.*429G>C ENSP00000442831.1:n.*429G>C
ENST00000537332.2:c.*429G>C ENSP00000444198.2:n.*429G>C
NM_001168388.2:c.*429G>C NP_001161860.1:n.*429G>C
NM_001168389.2:c.*429G>C NP_001161861.2:n.*429G>C
NM_006079.4:c.*429G>C NP_006070.2:n.*429G>C
NM_006079.5:c.*429G>C MANE Select NP_006070.2:n.*429G>C
NM_001168388.3:c.*429G>C NP_001161860.1:n.*429G>C
NM_001168389.3:c.*429G>C NP_001161861.2:n.*429G>C
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