Canonical Allele Identifier: CA210190321

Gene: RPS24

Linked Data

• dbSNP Id: rs760152907
• gnomAD v4: 10-78033779-C-A
• MyVariant Identifiers: chr10:g.79793537C>A (hg19) ; chr10:g.78033779C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78033779C>A , CM000672.2:g.78033779C>A	GRCh38
NC_000010.10:g.79793537C>A , CM000672.1:g.79793537C>A	GRCh37
NC_000010.9:g.79463543C>A	NCBI36
NG_012633.1:g.5020C>A
NG_029648.1:g.762G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613865.5:c.-123C>A	ENSP00000478869.2:n.-123C>A
ENST00000435275.5:c.-123C>A	ENSP00000415549.1:n.-123C>A
ENST00000440692.5:c.-123C>A	ENSP00000414321.1:n.-123C>A
ENST00000613865.4:c.-123C>A	ENSP00000478869.1:n.-123C>A
NM_001026.4:c.-123C>A	NP_001017.1:n.-123C>A
NM_001142282.1:c.-123C>A	NP_001135754.1:n.-123C>A
NM_001142283.1:c.-123C>A	NP_001135755.1:n.-123C>A
NM_001142284.1:c.-123C>A	NP_001135756.1:n.-123C>A
NM_001142285.1:c.-123C>A	NP_001135757.1:n.-123C>A
NM_033022.3:c.-123C>A	NP_148982.1:n.-123C>A