Canonical Allele Identifier: CA668640795

Gene: RPS24

Linked Data

• dbSNP Id: rs1272578418
• gnomAD v4: 10-78033774-T-C
• MyVariant Identifiers: chr10:g.79793532T>C (hg19) ; chr10:g.78033774T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78033774T>C , CM000672.2:g.78033774T>C	GRCh38
NC_000010.10:g.79793532T>C , CM000672.1:g.79793532T>C	GRCh37
NC_000010.9:g.79463538T>C	NCBI36
NG_012633.1:g.5015T>C
NG_029648.1:g.767A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613865.5:c.-128T>C	ENSP00000478869.2:n.-128T>C
ENST00000435275.5:c.-128T>C	ENSP00000415549.1:n.-128T>C
ENST00000440692.5:c.-128T>C	ENSP00000414321.1:n.-128T>C
ENST00000613865.4:c.-128T>C	ENSP00000478869.1:n.-128T>C
NM_001026.4:c.-128T>C	NP_001017.1:n.-128T>C
NM_001142282.1:c.-128T>C	NP_001135754.1:n.-128T>C
NM_001142283.1:c.-128T>C	NP_001135755.1:n.-128T>C
NM_001142284.1:c.-128T>C	NP_001135756.1:n.-128T>C
NM_001142285.1:c.-128T>C	NP_001135757.1:n.-128T>C
NM_033022.3:c.-128T>C	NP_148982.1:n.-128T>C