Canonical Allele Identifier: CA6621655

Gene: RPS26

Linked Data

• ClinVar Variation Id: 883851
• ClinVar RCV Id: RCV001114593 ; RCV004526081
• dbSNP Id: rs545595719
• ExAC: 12:56435962 T / A
• gnomAD v2: 12-56435962-T-A
• gnomAD v3: 12-56042178-T-A
• gnomAD v4: 12-56042178-T-A
• MyVariant Identifiers: chr12:g.56435962T>A (hg19) ; chr12:g.56042178T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56042178T>A , CM000674.2:g.56042178T>A	GRCh38
NC_000012.11:g.56435962T>A , CM000674.1:g.56435962T>A	GRCh37
NC_000012.10:g.54722229T>A	NCBI36
NG_023201.1:g.5277T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356464.10:c.3+9T>A	ENSP00000348849.5:n.3+9T>A
ENST00000646449.2:c.3+9T>A MANE Select	ENSP00000496643.1:n.3+9T>A
ENST00000356464.9:c.3+9T>A	ENSP00000348849.5:n.3+9T>A
ENST00000548590.1:n.30+9T>A
ENST00000552361.1:c.3+9T>A	ENSP00000450339.1:n.3+9T>A
NM_001029.3:c.3+9T>A	NP_001020.2:n.3+9T>A
NM_001029.5:c.3+9T>A MANE Select	NP_001020.2:n.3+9T>A