Canonical Allele Identifier: CA378379742
Gene: RBM20 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110780964G>C , CM000672.2:g.110780964G>C GRCh38
NC_000010.10:g.112540722G>C , CM000672.1:g.112540722G>C GRCh37
NC_000010.9:g.112530712G>C NCBI36
NG_021177.1:g.141568G>C , LRG_382:g.141568G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369519.4:c.355G>C MANE Select ENSP00000358532.3:p.Val119Leu
ENST00000369519.3:c.355G>C ENSP00000358532.3:p.Val119Leu
NM_001134363.2:c.355G>C NP_001127835.2:p.Val119Leu
XM_011539697.1:c.-30G>C XP_011537999.1:n.-30G>C
XM_017016103.2:c.190G>C XP_016871592.1:p.Val64Leu
XM_017016104.2:c.-30G>C XP_016871593.1:n.-30G>C
NM_001134363.3:c.355G>C MANE Select NP_001127835.2:p.Val119Leu