Canonical Allele Identifier: CA471506605

Gene: RBM20

Linked Data

• MyVariant Identifiers: chr10:g.112540634C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110780876C>T , CM000672.2:g.110780876C>T	GRCh38
NC_000010.10:g.112540634C>T , CM000672.1:g.112540634C>T	GRCh37
NC_000010.9:g.112530624C>T	NCBI36
NG_021177.1:g.141480C>T , LRG_382:g.141480C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369519.4:c.267C>T MANE Select	ENSP00000358532.3:p.Leu89=
ENST00000369519.3:c.267C>T	ENSP00000358532.3:p.Leu89=
NM_001134363.2:c.267C>T	NP_001127835.2:p.Leu89=
XM_011539697.1:c.-118C>T	XP_011537999.1:n.-118C>T
XM_017016103.2:c.102C>T	XP_016871592.1:p.Leu34=
XM_017016104.2:c.-118C>T	XP_016871593.1:n.-118C>T
NM_001134363.3:c.267C>T MANE Select	NP_001127835.2:p.Leu89=