Canonical Allele Identifier: CA1123763
Gene: RPS27 HGNC NCBI

Linked Data

dbSNP Id: rs778881750
ExAC: 1:153963232 T / C
gnomAD v2: 1-153963232-T-C
gnomAD v4: 1-153990756-T-C
MyVariant Identifiers: chr1:g.153963232T>C (hg19) chr1:g.153990756T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153990756T>C , CM000663.2:g.153990756T>C GRCh38
NC_000001.10:g.153963232T>C , CM000663.1:g.153963232T>C GRCh37
NC_000001.9:g.152229856T>C NCBI36
NG_053102.2:g.5002T>C

Transcript Alleles

HGVS Amino-acid Change
NM_001349946.1:c.-258T>C NP_001336875.1:n.-258T>C
NM_001349947.1:c.-369T>C NP_001336876.1:n.-369T>C
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