Canonical Allele Identifier: CA480184466
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs1425704800
gnomAD v2: 12-56435497-A-G
gnomAD v3: 12-56041713-A-G
gnomAD v4: 12-56041713-A-G
MyVariant Identifiers: chr12:g.56435497A>G (hg19) chr12:g.56041713A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041713A>G , CM000674.2:g.56041713A>G GRCh38
NC_000012.11:g.56435497A>G , CM000674.1:g.56435497A>G GRCh37
NC_000012.10:g.54721764A>G NCBI36
NG_023201.1:g.4812A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-98A>G ENSP00000348849.5:n.-356-98A>G
XR_944989.3:n.291T>C
XR_944990.3:n.291T>C
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