Canonical Allele Identifier: CA4025532
Gene: CITED2 HGNC NCBI

Linked Data

dbSNP Id: rs778782236

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.139373280A>C , CM000668.2:g.139373280A>C GRCh38
NC_000006.11:g.139694417A>C , CM000668.1:g.139694417A>C GRCh37
NC_000006.10:g.139736110A>C NCBI36
NG_016169.1:g.6369T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367651.4:c.665T>G MANE Select ENSP00000356623.2:p.Phe222Cys
ENST00000367651.3:c.665T>G ENSP00000356623.2:p.Phe222Cys
ENST00000536159.2:c.665T>G ENSP00000442831.1:p.Phe222Cys
ENST00000537332.2:c.680T>G ENSP00000444198.2:p.Phe227Cys
ENST00000618718.1:c.494T>G ENSP00000479918.1:p.Phe165Cys
NM_001168388.2:c.665T>G NP_001161860.1:p.Phe222Cys
NM_001168389.2:c.680T>G NP_001161861.2:p.Phe227Cys
NM_006079.4:c.665T>G NP_006070.2:p.Phe222Cys
NM_006079.5:c.665T>G MANE Select NP_006070.2:p.Phe222Cys
NM_001168388.3:c.665T>G NP_001161860.1:p.Phe222Cys
NM_001168389.3:c.680T>G NP_001161861.2:p.Phe227Cys