Canonical Allele Identifier: CA148813768

Gene: CITED2

Linked Data

• dbSNP Id: rs566103695
• gnomAD v3: 6-139373024-A-G
• gnomAD v4: 6-139373024-A-G
• MyVariant Identifiers: chr6:g.139694161A>G (hg19) ; chr6:g.139373024A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373024A>G , CM000668.2:g.139373024A>G	GRCh38
NC_000006.11:g.139694161A>G , CM000668.1:g.139694161A>G	GRCh37
NC_000006.10:g.139735854A>G	NCBI36
NG_016169.1:g.6625T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.*108T>C MANE Select	ENSP00000356623.2:n.*108T>C
ENST00000367651.3:c.*108T>C	ENSP00000356623.2:n.*108T>C
ENST00000536159.2:c.*108T>C	ENSP00000442831.1:n.*108T>C
ENST00000537332.2:c.*108T>C	ENSP00000444198.2:n.*108T>C
NM_001168388.2:c.*108T>C	NP_001161860.1:n.*108T>C
NM_001168389.2:c.*108T>C	NP_001161861.2:n.*108T>C
NM_006079.4:c.*108T>C	NP_006070.2:n.*108T>C
NM_006079.5:c.*108T>C MANE Select	NP_006070.2:n.*108T>C
NM_001168388.3:c.*108T>C	NP_001161860.1:n.*108T>C
NM_001168389.3:c.*108T>C	NP_001161861.2:n.*108T>C