Canonical Allele Identifier: CA378373642

Gene: RBM20

Linked Data

• MyVariant Identifiers: chr10:g.112572535A>T (hg19) ; chr10:g.110812777A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110812777A>T , CM000672.2:g.110812777A>T	GRCh38
NC_000010.10:g.112572535A>T , CM000672.1:g.112572535A>T	GRCh37
NC_000010.9:g.112562525A>T	NCBI36
NG_021177.1:g.173381A>T , LRG_382:g.173381A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000369519.4:c.2380A>T MANE Select	ENSP00000358532.3:p.Arg794Ter
ENST00000369519.3:c.2380A>T	ENSP00000358532.3:p.Arg794Ter
NM_001134363.2:c.2380A>T	NP_001127835.2:p.Arg794Ter
XM_011539697.1:c.1996A>T	XP_011537999.1:p.Arg666Ter
XM_017016103.2:c.2215A>T	XP_016871592.1:p.Arg739Ter
XM_017016104.2:c.1996A>T	XP_016871593.1:p.Arg666Ter
NM_001134363.3:c.2380A>T MANE Select	NP_001127835.2:p.Arg794Ter