Canonical Allele Identifier: CA2619258655

Gene: RPS26

Linked Data

• gnomAD v4: 12-56041780-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56041783_56041784del , CM000674.2:g.56041783_56041784del	GRCh38
NC_000012.11:g.56435567_56435568del , CM000674.1:g.56435567_56435568del	GRCh37
NC_000012.10:g.54721834_54721835del	NCBI36
NG_023201.1:g.4882_4883del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356464.10:c.-356-28_-356-27del	ENSP00000348849.5:n.-356-28_-356-27del
XR_944989.3:n.222_223del
XR_944990.3:n.222_223del