Canonical Allele Identifier: CA378370405
Gene: RBM20 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.112572086C>A (hg19) chr10:g.110812328C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110812328C>A , CM000672.2:g.110812328C>A GRCh38
NC_000010.10:g.112572086C>A , CM000672.1:g.112572086C>A GRCh37
NC_000010.9:g.112562076C>A NCBI36
NG_021177.1:g.172932C>A , LRG_382:g.172932C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369519.4:c.1931C>A MANE Select ENSP00000358532.3:p.Ser644Tyr
ENST00000369519.3:c.1931C>A ENSP00000358532.3:p.Ser644Tyr
NM_001134363.2:c.1931C>A NP_001127835.2:p.Ser644Tyr
XM_011539697.1:c.1547C>A XP_011537999.1:p.Ser516Tyr
XM_017016103.2:c.1766C>A XP_016871592.1:p.Ser589Tyr
XM_017016104.2:c.1547C>A XP_016871593.1:p.Ser516Tyr
NM_001134363.3:c.1931C>A MANE Select NP_001127835.2:p.Ser644Tyr
Search 100 bp 5'
Search 100 bp 3'