Canonical Allele Identifier: CA378527235
Gene: RBM20 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.112404217T>A (hg19) chr10:g.110644459T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110644459T>A , CM000672.2:g.110644459T>A GRCh38
NC_000010.10:g.112404217T>A , CM000672.1:g.112404217T>A GRCh37
NC_000010.9:g.112394207T>A NCBI36
NG_021177.1:g.5063T>A , LRG_382:g.5063T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369519.4:c.5T>A MANE Select ENSP00000358532.3:p.Val2Glu
ENST00000369519.3:c.5T>A ENSP00000358532.3:p.Val2Glu
NM_001134363.2:c.5T>A NP_001127835.2:p.Val2Glu
XM_017016103.2:c.26+1019T>A XP_016871592.1:n.26+1019T>A
NM_001134363.3:c.5T>A MANE Select NP_001127835.2:p.Val2Glu
Search 100 bp 5'
Search 100 bp 3'