Canonical Allele Identifier: CA1123765
Gene: RPS27 HGNC NCBI

Linked Data

dbSNP Id: rs758233900
ExAC: 1:153963234 C / T
gnomAD v2: 1-153963234-C-T
gnomAD v3: 1-153990758-C-T
gnomAD v4: 1-153990758-C-T
MyVariant Identifiers: chr1:g.153963234C>T (hg19) chr1:g.153990758C>T (hg38)
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Genomic Alleles

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

Transcript Alleles

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