Canonical Allele Identifier: CA690167307
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs1243185853
gnomAD v3: 12-56041966-A-C
gnomAD v4: 12-56041966-A-C
MyVariant Identifiers: chr12:g.56435750A>C (hg19) chr12:g.56041966A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041966A>C , CM000674.2:g.56041966A>C GRCh38
NC_000012.11:g.56435750A>C , CM000674.1:g.56435750A>C GRCh37
NC_000012.10:g.54722017A>C NCBI36
NG_023201.1:g.5065A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-201A>C ENSP00000348849.5:n.-201A>C
ENST00000646449.2:c.-201A>C MANE Select ENSP00000496643.1:n.-201A>C
ENST00000356464.9:c.-201A>C ENSP00000348849.5:n.-201A>C
ENST00000552361.1:c.-133A>C ENSP00000450339.1:n.-133A>C
NM_001029.3:c.-201A>C NP_001020.2:n.-201A>C
NM_001029.5:c.-201A>C MANE Select NP_001020.2:n.-201A>C
XR_944989.3:n.38T>G
XR_944990.3:n.38T>G
Search 100 bp 5'
Search 100 bp 3'