Canonical Allele Identifier: CA237623411

Gene: RPS26

Linked Data

• dbSNP Id: rs1032992797
• MyVariant Identifiers: chr12:g.56435365G>A (hg19) ; chr12:g.56041581G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56041581G>A , CM000674.2:g.56041581G>A	GRCh38
NC_000012.11:g.56435365G>A , CM000674.1:g.56435365G>A	GRCh37
NC_000012.10:g.54721632G>A	NCBI36
NG_023201.1:g.4680G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356464.10:c.-357+185G>A	ENSP00000348849.5:n.-357+185G>A
XR_944989.1:n.132C>T
XR_944990.1:n.132C>T
XR_944989.3:n.423C>T
XR_944990.3:n.423C>T