Canonical Allele Identifier: CA10636086

Gene: RPS24

Linked Data

• ClinVar Variation Id: 301088
• ClinVar RCV Id: RCV000274775 ; RCV000290077 ; RCV001108353
• dbSNP Id: rs3740254
• gnomAD v2: 10-79793551-A-G
• gnomAD v3: 10-78033793-A-G
• gnomAD v4: 10-78033793-A-G
• MyVariant Identifiers: chr10:g.79793551A>G (hg19) ; chr10:g.78033793A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78033793A>G , CM000672.2:g.78033793A>G	GRCh38
NC_000010.10:g.79793551A>G , CM000672.1:g.79793551A>G	GRCh37
NC_000010.9:g.79463557A>G	NCBI36
NG_012633.1:g.5034A>G
NG_029648.1:g.748T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613865.5:c.-109A>G	ENSP00000478869.2:n.-109A>G
ENST00000435275.5:c.-109A>G	ENSP00000415549.1:n.-109A>G
ENST00000440692.5:c.-109A>G	ENSP00000414321.1:n.-109A>G
ENST00000613865.4:c.-109A>G	ENSP00000478869.1:n.-109A>G
NM_001026.4:c.-109A>G	NP_001017.1:n.-109A>G
NM_001142282.1:c.-109A>G	NP_001135754.1:n.-109A>G
NM_001142283.1:c.-109A>G	NP_001135755.1:n.-109A>G
NM_001142284.1:c.-109A>G	NP_001135756.1:n.-109A>G
NM_001142285.1:c.-109A>G	NP_001135757.1:n.-109A>G
NM_033022.3:c.-109A>G	NP_148982.1:n.-109A>G