Canonical Allele Identifier: CA2038229710

Gene: RPS26

Linked Data

• dbSNP Id: rs1895894067

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56042165A>C , CM000674.2:g.56042165A>C	GRCh38
NC_000012.11:g.56435949A>C , CM000674.1:g.56435949A>C	GRCh37
NC_000012.10:g.54722216A>C	NCBI36
NG_023201.1:g.5264A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356464.10:c.-2A>C	ENSP00000348849.5:n.-2A>C
ENST00000646449.2:c.-2A>C MANE Select	ENSP00000496643.1:n.-2A>C
ENST00000356464.9:c.-2A>C	ENSP00000348849.5:n.-2A>C
ENST00000548590.1:n.26A>C
ENST00000552361.1:c.-2A>C	ENSP00000450339.1:n.-2A>C
NM_001029.3:c.-2A>C	NP_001020.2:n.-2A>C
NM_001029.5:c.-2A>C MANE Select	NP_001020.2:n.-2A>C