Canonical Allele Identifier: CA452441772

Gene: CITED2

Linked Data

• gnomAD v4: 6-139373444-G-T
• MyVariant Identifiers: chr6:g.139694581G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373444G>T , CM000668.2:g.139373444G>T	GRCh38
NC_000006.11:g.139694581G>T , CM000668.1:g.139694581G>T	GRCh37
NC_000006.10:g.139736274G>T	NCBI36
NG_016169.1:g.6205C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.501C>A MANE Select	ENSP00000356623.2:p.Pro167=
ENST00000367651.3:c.501C>A	ENSP00000356623.2:p.Pro167=
ENST00000536159.2:c.501C>A	ENSP00000442831.1:p.Pro167=
ENST00000537332.2:c.516C>A	ENSP00000444198.2:p.Pro172=
ENST00000618718.1:c.476+25C>A	ENSP00000479918.1:n.476+25C>A
NM_001168388.2:c.501C>A	NP_001161860.1:p.Pro167=
NM_001168389.2:c.516C>A	NP_001161861.2:p.Pro172=
NM_006079.4:c.501C>A	NP_006070.2:p.Pro167=
NM_006079.5:c.501C>A MANE Select	NP_006070.2:p.Pro167=
NM_001168388.3:c.501C>A	NP_001161860.1:p.Pro167=
NM_001168389.3:c.516C>A	NP_001161861.2:p.Pro172=