Canonical Allele Identifier: CA378379722
Gene: RBM20 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110780962C>A , CM000672.2:g.110780962C>A GRCh38
NC_000010.10:g.112540720C>A , CM000672.1:g.112540720C>A GRCh37
NC_000010.9:g.112530710C>A NCBI36
NG_021177.1:g.141566C>A , LRG_382:g.141566C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369519.4:c.353C>A MANE Select ENSP00000358532.3:p.Thr118Lys
ENST00000369519.3:c.353C>A ENSP00000358532.3:p.Thr118Lys
NM_001134363.2:c.353C>A NP_001127835.2:p.Thr118Lys
XM_011539697.1:c.-32C>A XP_011537999.1:n.-32C>A
XM_017016103.2:c.188C>A XP_016871592.1:p.Thr63Lys
XM_017016104.2:c.-32C>A XP_016871593.1:n.-32C>A
NM_001134363.3:c.353C>A MANE Select NP_001127835.2:p.Thr118Lys