Canonical Allele Identifier: CA213223665
Gene: RBM20 HGNC NCBI

Linked Data

ClinVar Variation Id: 1784074
ClinVar RCV Id: RCV002417011 RCV003097413
dbSNP Id: rs202011408
gnomAD v2: 10-112572152-G-A
gnomAD v3: 10-110812394-G-A
gnomAD v4: 10-110812394-G-A
MyVariant Identifiers: chr10:g.112572152G>A (hg19) chr10:g.110812394G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110812394G>A , CM000672.2:g.110812394G>A GRCh38
NC_000010.10:g.112572152G>A , CM000672.1:g.112572152G>A GRCh37
NC_000010.9:g.112562142G>A NCBI36
NG_021177.1:g.172998G>A , LRG_382:g.172998G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369519.4:c.1997G>A MANE Select ENSP00000358532.3:p.Arg666Gln
ENST00000369519.3:c.1997G>A ENSP00000358532.3:p.Arg666Gln
NM_001134363.2:c.1997G>A NP_001127835.2:p.Arg666Gln
XM_011539697.1:c.1613G>A XP_011537999.1:p.Arg538Gln
XM_017016103.2:c.1832G>A XP_016871592.1:p.Arg611Gln
XM_017016104.2:c.1613G>A XP_016871593.1:p.Arg538Gln
NM_001134363.3:c.1997G>A MANE Select NP_001127835.2:p.Arg666Gln
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