Canonical Allele Identifier: CA237623392
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs1000569422
MyVariant Identifiers: chr12:g.56435332T>C (hg19) chr12:g.56041548T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041548T>C , CM000674.2:g.56041548T>C GRCh38
NC_000012.11:g.56435332T>C , CM000674.1:g.56435332T>C GRCh37
NC_000012.10:g.54721599T>C NCBI36
NG_023201.1:g.4647T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-357+152T>C ENSP00000348849.5:n.-357+152T>C
XR_944989.1:n.165A>G
XR_944990.1:n.165A>G
XR_944989.3:n.456A>G
XR_944990.3:n.456A>G
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