Canonical Allele Identifier: CA471506404
Gene: RBM20 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.112540727G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110780969G>A , CM000672.2:g.110780969G>A GRCh38
NC_000010.10:g.112540727G>A , CM000672.1:g.112540727G>A GRCh37
NC_000010.9:g.112530717G>A NCBI36
NG_021177.1:g.141573G>A , LRG_382:g.141573G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369519.4:c.360G>A MANE Select ENSP00000358532.3:p.Leu120=
ENST00000369519.3:c.360G>A ENSP00000358532.3:p.Leu120=
NM_001134363.2:c.360G>A NP_001127835.2:p.Leu120=
XM_011539697.1:c.-25G>A XP_011537999.1:n.-25G>A
XM_017016103.2:c.195G>A XP_016871592.1:p.Leu65=
XM_017016104.2:c.-25G>A XP_016871593.1:n.-25G>A
NM_001134363.3:c.360G>A MANE Select NP_001127835.2:p.Leu120=