Canonical Allele Identifier: CA213223986
Gene: RBM20 HGNC NCBI

Linked Data

ClinVar Variation Id: 842533
ClinVar RCV Id: RCV001044964 RCV002429605
dbSNP Id: rs985340296
gnomAD v2: 10-112572380-C-G
gnomAD v3: 10-110812622-C-G
gnomAD v4: 10-110812622-C-G
MyVariant Identifiers: chr10:g.112572380C>G (hg19) chr10:g.110812622C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110812622C>G , CM000672.2:g.110812622C>G GRCh38
NC_000010.10:g.112572380C>G , CM000672.1:g.112572380C>G GRCh37
NC_000010.9:g.112562370C>G NCBI36
NG_021177.1:g.173226C>G , LRG_382:g.173226C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369519.4:c.2225C>G MANE Select ENSP00000358532.3:p.Ser742Cys
ENST00000369519.3:c.2225C>G ENSP00000358532.3:p.Ser742Cys
NM_001134363.2:c.2225C>G NP_001127835.2:p.Ser742Cys
XM_011539697.1:c.1841C>G XP_011537999.1:p.Ser614Cys
XM_017016103.2:c.2060C>G XP_016871592.1:p.Ser687Cys
XM_017016104.2:c.1841C>G XP_016871593.1:p.Ser614Cys
NM_001134363.3:c.2225C>G MANE Select NP_001127835.2:p.Ser742Cys
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