Canonical Allele Identifier: CA932504775
Gene: RBM20 HGNC NCBI

Linked Data

dbSNP Id: rs1861834042
gnomAD v3: 10-110644367-C-A
gnomAD v4: 10-110644367-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110644367C>A , CM000672.2:g.110644367C>A GRCh38
NC_000010.10:g.112404125C>A , CM000672.1:g.112404125C>A GRCh37
NC_000010.9:g.112394115C>A NCBI36
NG_021177.1:g.4971C>A , LRG_382:g.4971C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369519.4:c.-88C>A MANE Select ENSP00000358532.3:n.-88C>A
XM_017016103.2:c.26+927C>A XP_016871592.1:n.26+927C>A
NM_001134363.3:c.-88C>A MANE Select NP_001127835.2:n.-88C>A
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