Canonical Allele Identifier: CA13251998
Gene: RBM20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110667691C>T , CM000672.2:g.110667691C>T GRCh38
NC_000010.10:g.112427449C>T , CM000672.1:g.112427449C>T GRCh37
NC_000010.9:g.112417439C>T NCBI36
NG_021177.1:g.28295C>T , LRG_382:g.28295C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369519.4:c.191+23046C>T MANE Select ENSP00000358532.3:n.191+23046C>T
ENST00000369519.3:c.191+23046C>T ENSP00000358532.3:n.191+23046C>T
NM_001134363.2:c.191+23046C>T NP_001127835.2:n.191+23046C>T
XR_428811.2:n.158+198C>T
XM_017016103.2:c.26+24251C>T XP_016871592.1:n.26+24251C>T
NM_001134363.3:c.191+23046C>T MANE Select NP_001127835.2:n.191+23046C>T