Canonical Allele Identifier: CA819731518

Gene: CITED2

Linked Data

• dbSNP Id: rs1252068169
• gnomAD v3: 6-139372976-A-T
• gnomAD v4: 6-139372976-A-T
• MyVariant Identifiers: chr6:g.139694113A>T (hg19) ; chr6:g.139372976A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139372976A>T , CM000668.2:g.139372976A>T	GRCh38
NC_000006.11:g.139694113A>T , CM000668.1:g.139694113A>T	GRCh37
NC_000006.10:g.139735806A>T	NCBI36
NG_016169.1:g.6673T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.*156T>A MANE Select	ENSP00000356623.2:n.*156T>A
ENST00000367651.3:c.*156T>A	ENSP00000356623.2:n.*156T>A
ENST00000536159.2:c.*156T>A	ENSP00000442831.1:n.*156T>A
ENST00000537332.2:c.*156T>A	ENSP00000444198.2:n.*156T>A
NM_001168388.2:c.*156T>A	NP_001161860.1:n.*156T>A
NM_001168389.2:c.*156T>A	NP_001161861.2:n.*156T>A
NM_006079.4:c.*156T>A	NP_006070.2:n.*156T>A
NM_006079.5:c.*156T>A MANE Select	NP_006070.2:n.*156T>A
NM_001168388.3:c.*156T>A	NP_001161860.1:n.*156T>A
NM_001168389.3:c.*156T>A	NP_001161861.2:n.*156T>A