Canonical Allele Identifier: CA1123771
Gene: RPS27 HGNC NCBI

Linked Data

dbSNP Id: rs151191078
ExAC: 1:153963236 C / A
gnomAD v2: 1-153963236-C-A
gnomAD v3: 1-153990760-C-A
gnomAD v4: 1-153990760-C-A
COSMIC: COSN26645490
MyVariant Identifiers: chr1:g.153963236C>A (hg19) chr1:g.153990760C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153990760C>A , CM000663.2:g.153990760C>A GRCh38
NC_000001.10:g.153963236C>A , CM000663.1:g.153963236C>A GRCh37
NC_000001.9:g.152229860C>A NCBI36
NG_053102.2:g.5006C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368567.4:c.-37C>A ENSP00000357555.4:n.-37C>A
NM_001349946.1:c.-254C>A NP_001336875.1:n.-254C>A
NM_001349947.1:c.-365C>A NP_001336876.1:n.-365C>A
Search 100 bp 5'
Search 100 bp 3'