Canonical Allele Identifier: CA2555338478
Gene: RBM20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110644355G>C , CM000672.2:g.110644355G>C GRCh38
NC_000010.10:g.112404113G>C , CM000672.1:g.112404113G>C GRCh37
NC_000010.9:g.112394103G>C NCBI36
NG_021177.1:g.4959G>C , LRG_382:g.4959G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369519.4:c.-100G>C MANE Select ENSP00000358532.3:n.-100G>C
XM_017016103.2:c.26+915G>C XP_016871592.1:n.26+915G>C
NM_001134363.3:c.-100G>C MANE Select NP_001127835.2:n.-100G>C