Canonical Allele Identifier: CA1123766
Gene: RPS27 HGNC NCBI

Linked Data

dbSNP Id: rs758233900
ExAC: 1:153963234 C / A
gnomAD v2: 1-153963234-C-A
gnomAD v4: 1-153990758-C-A
MyVariant Identifiers: chr1:g.153963234C>A (hg19) chr1:g.153990758C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153990758C>A , CM000663.2:g.153990758C>A GRCh38
NC_000001.10:g.153963234C>A , CM000663.1:g.153963234C>A GRCh37
NC_000001.9:g.152229858C>A NCBI36
NG_053102.2:g.5004C>A

Transcript Alleles

HGVS Amino-acid Change
NM_001349946.1:c.-256C>A NP_001336875.1:n.-256C>A
NM_001349947.1:c.-367C>A NP_001336876.1:n.-367C>A
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