Canonical Allele Identifier: CA2619259103
Gene: RPS26 HGNC NCBI

Linked Data

gnomAD v4: 12-56042129-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56042129C>T , CM000674.2:g.56042129C>T GRCh38
NC_000012.11:g.56435913C>T , CM000674.1:g.56435913C>T GRCh37
NC_000012.10:g.54722180C>T NCBI36
NG_023201.1:g.5228C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-38C>T ENSP00000348849.5:n.-38C>T
ENST00000646449.2:c.-38C>T MANE Select ENSP00000496643.1:n.-38C>T
ENST00000356464.9:c.-38C>T ENSP00000348849.5:n.-38C>T
ENST00000552361.1:c.-34-4C>T ENSP00000450339.1:n.-34-4C>T
NM_001029.3:c.-38C>T NP_001020.2:n.-38C>T
NM_001029.5:c.-38C>T MANE Select NP_001020.2:n.-38C>T
Search 100 bp 5'
Search 100 bp 3'