Canonical Allele Identifier: CA2580967529

Gene: RBM20

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110812311G= , CM000672.2:g.110812311G=	GRCh38
NC_000010.10:g.112572069G= , CM000672.1:g.112572069G=	GRCh37
NC_000010.9:g.112562059G=	NCBI36
NG_021177.1:g.172915G= , LRG_382:g.172915G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000369519.4:c.1914G= MANE Select	ENSP00000358532.3:p.Pro638=
ENST00000369519.3:c.1914G=	ENSP00000358532.3:p.Pro638=
NM_001134363.2:c.1914G=	NP_001127835.2:p.Pro638=
XM_011539697.1:c.1530G=	XP_011537999.1:p.Pro510=
XM_017016103.2:c.1749G=	XP_016871592.1:p.Pro583=
XM_017016104.2:c.1530G=	XP_016871593.1:p.Pro510=
NM_001134363.3:c.1914G= MANE Select	NP_001127835.2:p.Pro638=