Canonical Allele Identifier: CA471368132

Gene: RBM20

Linked Data

• MyVariant Identifiers: chr10:g.112572192T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110812434T>G , CM000672.2:g.110812434T>G	GRCh38
NC_000010.10:g.112572192T>G , CM000672.1:g.112572192T>G	GRCh37
NC_000010.9:g.112562182T>G	NCBI36
NG_021177.1:g.173038T>G , LRG_382:g.173038T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369519.4:c.2037T>G MANE Select	ENSP00000358532.3:p.Ser679=
ENST00000369519.3:c.2037T>G	ENSP00000358532.3:p.Ser679=
NM_001134363.2:c.2037T>G	NP_001127835.2:p.Ser679=
XM_011539697.1:c.1653T>G	XP_011537999.1:p.Ser551=
XM_017016103.2:c.1872T>G	XP_016871592.1:p.Ser624=
XM_017016104.2:c.1653T>G	XP_016871593.1:p.Ser551=
NM_001134363.3:c.2037T>G MANE Select	NP_001127835.2:p.Ser679=