Canonical Allele Identifier: CA2619258058
Gene: RPS26 HGNC NCBI

Linked Data

gnomAD v4: 12-56041568-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041568G>T , CM000674.2:g.56041568G>T GRCh38
NC_000012.11:g.56435352G>T , CM000674.1:g.56435352G>T GRCh37
NC_000012.10:g.54721619G>T NCBI36
NG_023201.1:g.4667G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-357+172G>T ENSP00000348849.5:n.-357+172G>T
XR_944989.1:n.145C>A
XR_944990.1:n.145C>A
XR_944989.3:n.436C>A
XR_944990.3:n.436C>A
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