Canonical Allele Identifier: CA1123768
Gene: RPS27 HGNC NCBI

Linked Data

dbSNP Id: rs746666834
ExAC: 1:153963235 G / C
gnomAD v2: 1-153963235-G-C
gnomAD v3: 1-153990759-G-C
gnomAD v4: 1-153990759-G-C
MyVariant Identifiers: chr1:g.153963235G>C (hg19) chr1:g.153990759G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153990759G>C , CM000663.2:g.153990759G>C GRCh38
NC_000001.10:g.153963235G>C , CM000663.1:g.153963235G>C GRCh37
NC_000001.9:g.152229859G>C NCBI36
NG_053102.2:g.5005G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368567.4:c.-38G>C ENSP00000357555.4:n.-38G>C
NM_001349946.1:c.-255G>C NP_001336875.1:n.-255G>C
NM_001349947.1:c.-366G>C NP_001336876.1:n.-366G>C
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