Canonical Allele Identifier: CA2038229525
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs1895890784
gnomAD v4: 12-56042081-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56042081T>G , CM000674.2:g.56042081T>G GRCh38
NC_000012.11:g.56435865T>G , CM000674.1:g.56435865T>G GRCh37
NC_000012.10:g.54722132T>G NCBI36
NG_023201.1:g.5180T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000356464.10:c.-86T>G ENSP00000348849.5:n.-86T>G
ENST00000646449.2:c.-86T>G MANE Select ENSP00000496643.1:n.-86T>G
ENST00000356464.9:c.-86T>G ENSP00000348849.5:n.-86T>G
ENST00000552361.1:c.-35+17T>G ENSP00000450339.1:n.-35+17T>G
NM_001029.3:c.-86T>G NP_001020.2:n.-86T>G
NM_001029.5:c.-86T>G MANE Select NP_001020.2:n.-86T>G
Search 100 bp 5'
Search 100 bp 3'