Canonical Allele Identifier: CA365876006

Gene: CITED2

Linked Data

• gnomAD v4: 6-139373154-T-G
• MyVariant Identifiers: chr6:g.139694291T>G (hg19) ; chr6:g.139373154T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373154T>G , CM000668.2:g.139373154T>G	GRCh38
NC_000006.11:g.139694291T>G , CM000668.1:g.139694291T>G	GRCh37
NC_000006.10:g.139735984T>G	NCBI36
NG_016169.1:g.6495A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.791A>C MANE Select	ENSP00000356623.2:p.Gln264Pro
ENST00000367651.3:c.791A>C	ENSP00000356623.2:p.Gln264Pro
ENST00000536159.2:c.791A>C	ENSP00000442831.1:p.Gln264Pro
ENST00000537332.2:c.806A>C	ENSP00000444198.2:p.Gln269Pro
ENST00000618718.1:c.620A>C	ENSP00000479918.1:p.Gln207Pro
NM_001168388.2:c.791A>C	NP_001161860.1:p.Gln264Pro
NM_001168389.2:c.806A>C	NP_001161861.2:p.Gln269Pro
NM_006079.4:c.791A>C	NP_006070.2:p.Gln264Pro
NM_006079.5:c.791A>C MANE Select	NP_006070.2:p.Gln264Pro
NM_001168388.3:c.791A>C	NP_001161860.1:p.Gln264Pro
NM_001168389.3:c.806A>C	NP_001161861.2:p.Gln269Pro