Canonical Allele Identifier: CA237623611
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs893055492
gnomAD v3: 12-56041951-T-C
gnomAD v4: 12-56041951-T-C
MyVariant Identifiers: chr12:g.56435735T>C (hg19) chr12:g.56041951T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041951T>C , CM000674.2:g.56041951T>C GRCh38
NC_000012.11:g.56435735T>C , CM000674.1:g.56435735T>C GRCh37
NC_000012.10:g.54722002T>C NCBI36
NG_023201.1:g.5050T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-216T>C ENSP00000348849.5:n.-216T>C
ENST00000646449.2:c.-216T>C MANE Select ENSP00000496643.1:n.-216T>C
ENST00000356464.9:c.-216T>C ENSP00000348849.5:n.-216T>C
ENST00000552361.1:c.-148T>C ENSP00000450339.1:n.-148T>C
NM_001029.3:c.-216T>C NP_001020.2:n.-216T>C
NM_001029.5:c.-216T>C MANE Select NP_001020.2:n.-216T>C
XR_944989.3:n.53A>G
XR_944990.3:n.53A>G
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