Canonical Allele Identifier: CA480184366
Gene: RPS26 HGNC NCBI

Linked Data

gnomAD v4: 12-56041676-A-T
MyVariant Identifiers: chr12:g.56435460A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041676A>T , CM000674.2:g.56041676A>T GRCh38
NC_000012.11:g.56435460A>T , CM000674.1:g.56435460A>T GRCh37
NC_000012.10:g.54721727A>T NCBI36
NG_023201.1:g.4775A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-135A>T ENSP00000348849.5:n.-356-135A>T
XR_944989.1:n.37T>A
XR_944990.1:n.37T>A
XR_944989.3:n.328T>A
XR_944990.3:n.328T>A
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