Canonical Allele Identifier: CA668640835

Gene: RPS24

Linked Data

• dbSNP Id: rs1429967665
• gnomAD v3: 10-78033813-C-T
• gnomAD v4: 10-78033813-C-T
• MyVariant Identifiers: chr10:g.79793571C>T (hg19) ; chr10:g.78033813C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78033813C>T , CM000672.2:g.78033813C>T	GRCh38
NC_000010.10:g.79793571C>T , CM000672.1:g.79793571C>T	GRCh37
NC_000010.9:g.79463577C>T	NCBI36
NG_012633.1:g.5054C>T
NG_029648.1:g.728G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613865.5:c.-89C>T	ENSP00000478869.2:n.-89C>T
ENST00000435275.5:c.-89C>T	ENSP00000415549.1:n.-89C>T
ENST00000440692.5:c.-89C>T	ENSP00000414321.1:n.-89C>T
ENST00000613865.4:c.-89C>T	ENSP00000478869.1:n.-89C>T
NM_001026.4:c.-89C>T	NP_001017.1:n.-89C>T
NM_001142282.1:c.-89C>T	NP_001135754.1:n.-89C>T
NM_001142283.1:c.-89C>T	NP_001135755.1:n.-89C>T
NM_001142284.1:c.-89C>T	NP_001135756.1:n.-89C>T
NM_001142285.1:c.-89C>T	NP_001135757.1:n.-89C>T
NM_033022.3:c.-89C>T	NP_148982.1:n.-89C>T