Canonical Allele Identifier: CA2680562453

Gene: CITED2

Linked Data

• gnomAD v4: 6-139372980-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139372980C>A , CM000668.2:g.139372980C>A	GRCh38
NC_000006.11:g.139694117C>A , CM000668.1:g.139694117C>A	GRCh37
NC_000006.10:g.139735810C>A	NCBI36
NG_016169.1:g.6669G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.*152G>T MANE Select	ENSP00000356623.2:n.*152G>T
ENST00000367651.3:c.*152G>T	ENSP00000356623.2:n.*152G>T
ENST00000536159.2:c.*152G>T	ENSP00000442831.1:n.*152G>T
ENST00000537332.2:c.*152G>T	ENSP00000444198.2:n.*152G>T
NM_001168388.2:c.*152G>T	NP_001161860.1:n.*152G>T
NM_001168389.2:c.*152G>T	NP_001161861.2:n.*152G>T
NM_006079.4:c.*152G>T	NP_006070.2:n.*152G>T
NM_006079.5:c.*152G>T MANE Select	NP_006070.2:n.*152G>T
NM_001168388.3:c.*152G>T	NP_001161860.1:n.*152G>T
NM_001168389.3:c.*152G>T	NP_001161861.2:n.*152G>T