Canonical Allele Identifier: CA237623431
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs998070148
gnomAD v2: 12-56435413-TAGA-T
gnomAD v4: 12-56041629-TAGA-T
MyVariant Identifiers: chr12:g.56435414_56435416del (hg19) chr12:g.56041630_56041632del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041632_56041634del , CM000674.2:g.56041632_56041634del GRCh38
NC_000012.11:g.56435416_56435418del , CM000674.1:g.56435416_56435418del GRCh37
NC_000012.10:g.54721683_54721685del NCBI36
NG_023201.1:g.4731_4733del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-179_-356-177del ENSP00000348849.5:n.-356-179_-356-177del
XR_944989.1:n.81_83del
XR_944990.1:n.81_83del
XR_944989.3:n.372_374del
XR_944990.3:n.372_374del
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