Canonical Allele Identifier: CA4025543

Gene: CITED2

Linked Data

• ClinVar Variation Id: 733119
• ClinVar RCV Id: RCV000908356
• dbSNP Id: rs767902739
• ExAC: 6:139694455 G / A
• gnomAD v2: 6-139694455-G-A
• gnomAD v3: 6-139373318-G-A
• gnomAD v4: 6-139373318-G-A
• MyVariant Identifiers: chr6:g.139694455G>A (hg19) ; chr6:g.139373318G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373318G>A , CM000668.2:g.139373318G>A	GRCh38
NC_000006.11:g.139694455G>A , CM000668.1:g.139694455G>A	GRCh37
NC_000006.10:g.139736148G>A	NCBI36
NG_016169.1:g.6331C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.627C>T MANE Select	ENSP00000356623.2:p.Pro209=
ENST00000367651.3:c.627C>T	ENSP00000356623.2:p.Pro209=
ENST00000536159.2:c.627C>T	ENSP00000442831.1:p.Pro209=
ENST00000537332.2:c.642C>T	ENSP00000444198.2:p.Pro214=
ENST00000618718.1:c.477-21C>T	ENSP00000479918.1:n.477-21C>T
NM_001168388.2:c.627C>T	NP_001161860.1:p.Pro209=
NM_001168389.2:c.642C>T	NP_001161861.2:p.Pro214=
NM_006079.4:c.627C>T	NP_006070.2:p.Pro209=
NM_006079.5:c.627C>T MANE Select	NP_006070.2:p.Pro209=
NM_001168388.3:c.627C>T	NP_001161860.1:p.Pro209=
NM_001168389.3:c.642C>T	NP_001161861.2:p.Pro214=