Canonical Allele Identifier: CA605259069

Gene: RPS26

Linked Data

• dbSNP Id: rs1261382167
• gnomAD v2: 12-56435403-AC-A
• gnomAD v3: 12-56041619-AC-A
• gnomAD v4: 12-56041619-AC-A
• MyVariant Identifiers: chr12:g.56435404del (hg19) ; chr12:g.56041620del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56041621del , CM000674.2:g.56041621del	GRCh38
NC_000012.11:g.56435405del , CM000674.1:g.56435405del	GRCh37
NC_000012.10:g.54721672del	NCBI36
NG_023201.1:g.4720del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356464.10:c.-356-190del	ENSP00000348849.5:n.-356-190del
XR_944989.1:n.93del
XR_944990.1:n.93del
XR_944989.3:n.384del
XR_944990.3:n.384del