Canonical Allele Identifier: CA237623416
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs375444321
gnomAD v2: 12-56435374-C-T
gnomAD v3: 12-56041590-C-T
gnomAD v4: 12-56041590-C-T
MyVariant Identifiers: chr12:g.56435374C>T (hg19) chr12:g.56041590C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041590C>T , CM000674.2:g.56041590C>T GRCh38
NC_000012.11:g.56435374C>T , CM000674.1:g.56435374C>T GRCh37
NC_000012.10:g.54721641C>T NCBI36
NG_023201.1:g.4689C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-357+194C>T ENSP00000348849.5:n.-357+194C>T
XR_944989.1:n.123G>A
XR_944990.1:n.123G>A
XR_944989.3:n.414G>A
XR_944990.3:n.414G>A
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