Canonical Allele Identifier: CA2038229344
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs1895887619
gnomAD v4: 12-56041914-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041914C>T , CM000674.2:g.56041914C>T GRCh38
NC_000012.11:g.56435698C>T , CM000674.1:g.56435698C>T GRCh37
NC_000012.10:g.54721965C>T NCBI36
NG_023201.1:g.5013C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-253C>T ENSP00000348849.5:n.-253C>T
ENST00000356464.9:c.-253C>T ENSP00000348849.5:n.-253C>T
ENST00000552361.1:c.-185C>T ENSP00000450339.1:n.-185C>T
NM_001029.3:c.-253C>T NP_001020.2:n.-253C>T
XR_944989.3:n.90G>A
XR_944990.3:n.90G>A
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