Canonical Allele Identifier: CA365876699
Gene: CITED2 HGNC NCBI

Linked Data

dbSNP Id: rs1323551506

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.139373374T>C , CM000668.2:g.139373374T>C GRCh38
NC_000006.11:g.139694511T>C , CM000668.1:g.139694511T>C GRCh37
NC_000006.10:g.139736204T>C NCBI36
NG_016169.1:g.6275A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367651.4:c.571A>G MANE Select ENSP00000356623.2:p.Asn191Asp
ENST00000367651.3:c.571A>G ENSP00000356623.2:p.Asn191Asp
ENST00000536159.2:c.571A>G ENSP00000442831.1:p.Asn191Asp
ENST00000537332.2:c.586A>G ENSP00000444198.2:p.Asn196Asp
ENST00000618718.1:c.477-77A>G ENSP00000479918.1:n.477-77A>G
NM_001168388.2:c.571A>G NP_001161860.1:p.Asn191Asp
NM_001168389.2:c.586A>G NP_001161861.2:p.Asn196Asp
NM_006079.4:c.571A>G NP_006070.2:p.Asn191Asp
NM_006079.5:c.571A>G MANE Select NP_006070.2:p.Asn191Asp
NM_001168388.3:c.571A>G NP_001161860.1:p.Asn191Asp
NM_001168389.3:c.586A>G NP_001161861.2:p.Asn196Asp