Canonical Allele Identifier: CA2619259140
Gene: RPS26 HGNC NCBI

Linked Data

gnomAD v4: 12-56042180-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56042180T>A , CM000674.2:g.56042180T>A GRCh38
NC_000012.11:g.56435964T>A , CM000674.1:g.56435964T>A GRCh37
NC_000012.10:g.54722231T>A NCBI36
NG_023201.1:g.5279T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.3+11T>A ENSP00000348849.5:n.3+11T>A
ENST00000646449.2:c.3+11T>A MANE Select ENSP00000496643.1:n.3+11T>A
ENST00000356464.9:c.3+11T>A ENSP00000348849.5:n.3+11T>A
ENST00000548590.1:n.30+11T>A
ENST00000552361.1:c.3+11T>A ENSP00000450339.1:n.3+11T>A
NM_001029.3:c.3+11T>A NP_001020.2:n.3+11T>A
NM_001029.5:c.3+11T>A MANE Select NP_001020.2:n.3+11T>A
Search 100 bp 5'
Search 100 bp 3'