Canonical Allele Identifier: CA2610889889
Gene: RBM20 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110644360C>A , CM000672.2:g.110644360C>A GRCh38
NC_000010.10:g.112404118C>A , CM000672.1:g.112404118C>A GRCh37
NC_000010.9:g.112394108C>A NCBI36
NG_021177.1:g.4964C>A , LRG_382:g.4964C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369519.4:c.-95C>A MANE Select ENSP00000358532.3:n.-95C>A
XM_017016103.2:c.26+920C>A XP_016871592.1:n.26+920C>A
NM_001134363.3:c.-95C>A MANE Select NP_001127835.2:n.-95C>A