Canonical Allele Identifier: CA480184384
Gene: RPS26 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.56435467C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041683C>T , CM000674.2:g.56041683C>T GRCh38
NC_000012.11:g.56435467C>T , CM000674.1:g.56435467C>T GRCh37
NC_000012.10:g.54721734C>T NCBI36
NG_023201.1:g.4782C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-128C>T ENSP00000348849.5:n.-356-128C>T
XR_944989.1:n.30G>A
XR_944990.1:n.30G>A
XR_944989.3:n.321G>A
XR_944990.3:n.321G>A
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