Canonical Allele Identifier: CA2680562489

Gene: CITED2

Linked Data

• gnomAD v4: 6-139373009-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373009G>A , CM000668.2:g.139373009G>A	GRCh38
NC_000006.11:g.139694146G>A , CM000668.1:g.139694146G>A	GRCh37
NC_000006.10:g.139735839G>A	NCBI36
NG_016169.1:g.6640C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.*123C>T MANE Select	ENSP00000356623.2:n.*123C>T
ENST00000367651.3:c.*123C>T	ENSP00000356623.2:n.*123C>T
ENST00000536159.2:c.*123C>T	ENSP00000442831.1:n.*123C>T
ENST00000537332.2:c.*123C>T	ENSP00000444198.2:n.*123C>T
NM_001168388.2:c.*123C>T	NP_001161860.1:n.*123C>T
NM_001168389.2:c.*123C>T	NP_001161861.2:n.*123C>T
NM_006079.4:c.*123C>T	NP_006070.2:n.*123C>T
NM_006079.5:c.*123C>T MANE Select	NP_006070.2:n.*123C>T
NM_001168388.3:c.*123C>T	NP_001161860.1:n.*123C>T
NM_001168389.3:c.*123C>T	NP_001161861.2:n.*123C>T