Canonical Allele Identifier: CA1123772
Gene: RPS27 HGNC NCBI

Linked Data

dbSNP Id: rs773902654
ExAC: 1:153963237 T / A
gnomAD v2: 1-153963237-T-A
gnomAD v4: 1-153990761-T-A
MyVariant Identifiers: chr1:g.153963237T>A (hg19) chr1:g.153990761T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153990761T>A , CM000663.2:g.153990761T>A GRCh38
NC_000001.10:g.153963237T>A , CM000663.1:g.153963237T>A GRCh37
NC_000001.9:g.152229861T>A NCBI36
NG_053102.2:g.5007T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368567.4:c.-36T>A ENSP00000357555.4:n.-36T>A
NM_001349946.1:c.-253T>A NP_001336875.1:n.-253T>A
NM_001349947.1:c.-364T>A NP_001336876.1:n.-364T>A
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