Canonical Allele Identifier: CA2575186524

Gene: RPS26

Linked Data

• gnomAD v4: 12-56042103-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56042103A>C , CM000674.2:g.56042103A>C	GRCh38
NC_000012.11:g.56435887A>C , CM000674.1:g.56435887A>C	GRCh37
NC_000012.10:g.54722154A>C	NCBI36
NG_023201.1:g.5202A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356464.10:c.-64A>C	ENSP00000348849.5:n.-64A>C
ENST00000646449.2:c.-64A>C MANE Select	ENSP00000496643.1:n.-64A>C
ENST00000356464.9:c.-64A>C	ENSP00000348849.5:n.-64A>C
ENST00000552361.1:c.-34-30A>C	ENSP00000450339.1:n.-34-30A>C
NM_001029.3:c.-64A>C	NP_001020.2:n.-64A>C
NM_001029.5:c.-64A>C MANE Select	NP_001020.2:n.-64A>C