Canonical Allele Identifier: CA605259200
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs1188199594
gnomAD v2: 12-56435961-T-A
MyVariant Identifiers: chr12:g.56435961T>A (hg19) chr12:g.56042177T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56042177T>A , CM000674.2:g.56042177T>A GRCh38
NC_000012.11:g.56435961T>A , CM000674.1:g.56435961T>A GRCh37
NC_000012.10:g.54722228T>A NCBI36
NG_023201.1:g.5276T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.3+8T>A ENSP00000348849.5:n.3+8T>A
ENST00000646449.2:c.3+8T>A MANE Select ENSP00000496643.1:n.3+8T>A
ENST00000356464.9:c.3+8T>A ENSP00000348849.5:n.3+8T>A
ENST00000548590.1:n.30+8T>A
ENST00000552361.1:c.3+8T>A ENSP00000450339.1:n.3+8T>A
NM_001029.3:c.3+8T>A NP_001020.2:n.3+8T>A
NM_001029.5:c.3+8T>A MANE Select NP_001020.2:n.3+8T>A
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