Canonical Allele Identifier: CA696955902

Gene: RPL21

Linked Data

• dbSNP Id: rs1226796807
• gnomAD v3: 13-27254053-T-C
• gnomAD v4: 13-27254053-T-C
• MyVariant Identifiers: chr13:g.27828190T>C (hg19) ; chr13:g.27254053T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.27254053T>C , CM000675.2:g.27254053T>C	GRCh38
NC_000013.10:g.27828190T>C , CM000675.1:g.27828190T>C	GRCh37
NC_000013.9:g.26726190T>C	NCBI36
NG_046927.1:g.7499T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311549.11:c.68-167T>C MANE Select	ENSP00000346027.4:n.68-167T>C
ENST00000272274.8:c.68-167T>C	ENSP00000351021.2:n.68-167T>C
ENST00000311549.10:c.68-167T>C	ENSP00000346027.4:n.68-167T>C
ENST00000319826.8:c.68-167T>C	ENSP00000370574.1:n.68-167T>C
ENST00000326092.8:c.68-167T>C	ENSP00000370569.1:n.68-167T>C
ENST00000461690.5:c.68-167T>C	ENSP00000434298.1:n.68-167T>C
ENST00000466550.1:n.80-167T>C
ENST00000473558.5:n.304-167T>C
ENST00000483765.5:c.67+210T>C	ENSP00000473246.1:n.67+210T>C
ENST00000493317.1:c.68-167T>C	ENSP00000471695.1:n.68-167T>C
NM_000982.3:c.68-167T>C	NP_000973.2:n.68-167T>C
NM_000982.4:c.68-167T>C MANE Select	NP_000973.2:n.68-167T>C