Canonical Allele Identifier: CA365876724

Gene: CITED2

Linked Data

• dbSNP Id: rs1778295631
• gnomAD v3: 6-139373386-C-A
• gnomAD v4: 6-139373386-C-A
• MyVariant Identifiers: chr6:g.139694523C>A (hg19) ; chr6:g.139373386C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373386C>A , CM000668.2:g.139373386C>A	GRCh38
NC_000006.11:g.139694523C>A , CM000668.1:g.139694523C>A	GRCh37
NC_000006.10:g.139736216C>A	NCBI36
NG_016169.1:g.6263G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.559G>T MANE Select	ENSP00000356623.2:p.Ala187Ser
ENST00000367651.3:c.559G>T	ENSP00000356623.2:p.Ala187Ser
ENST00000536159.2:c.559G>T	ENSP00000442831.1:p.Ala187Ser
ENST00000537332.2:c.574G>T	ENSP00000444198.2:p.Ala192Ser
ENST00000618718.1:c.476+83G>T	ENSP00000479918.1:n.476+83G>T
NM_001168388.2:c.559G>T	NP_001161860.1:p.Ala187Ser
NM_001168389.2:c.574G>T	NP_001161861.2:p.Ala192Ser
NM_006079.4:c.559G>T	NP_006070.2:p.Ala187Ser
NM_006079.5:c.559G>T MANE Select	NP_006070.2:p.Ala187Ser
NM_001168388.3:c.559G>T	NP_001161860.1:p.Ala187Ser
NM_001168389.3:c.574G>T	NP_001161861.2:p.Ala192Ser