Canonical Allele Identifier: CA148813723

Gene: CITED2

Linked Data

• dbSNP Id: rs1039463342
• gnomAD v2: 6-139693940-C-G
• gnomAD v3: 6-139372803-C-G
• gnomAD v4: 6-139372803-C-G
• MyVariant Identifiers: chr6:g.139693940C>G (hg19) ; chr6:g.139372803C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139372803C>G , CM000668.2:g.139372803C>G	GRCh38
NC_000006.11:g.139693940C>G , CM000668.1:g.139693940C>G	GRCh37
NC_000006.10:g.139735633C>G	NCBI36
NG_016169.1:g.6846G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.*329G>C MANE Select	ENSP00000356623.2:n.*329G>C
ENST00000367651.3:c.*329G>C	ENSP00000356623.2:n.*329G>C
ENST00000536159.2:c.*329G>C	ENSP00000442831.1:n.*329G>C
ENST00000537332.2:c.*329G>C	ENSP00000444198.2:n.*329G>C
NM_001168388.2:c.*329G>C	NP_001161860.1:n.*329G>C
NM_001168389.2:c.*329G>C	NP_001161861.2:n.*329G>C
NM_006079.4:c.*329G>C	NP_006070.2:n.*329G>C
NM_006079.5:c.*329G>C MANE Select	NP_006070.2:n.*329G>C
NM_001168388.3:c.*329G>C	NP_001161860.1:n.*329G>C
NM_001168389.3:c.*329G>C	NP_001161861.2:n.*329G>C