Canonical Allele Identifier: CA378379284

Gene: RBM20

Linked Data

• gnomAD v4: 10-110780875-T-C
• COSMIC: COSM3358626
• MyVariant Identifiers: chr10:g.112540633T>C (hg19) ; chr10:g.110780875T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110780875T>C , CM000672.2:g.110780875T>C	GRCh38
NC_000010.10:g.112540633T>C , CM000672.1:g.112540633T>C	GRCh37
NC_000010.9:g.112530623T>C	NCBI36
NG_021177.1:g.141479T>C , LRG_382:g.141479T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369519.4:c.266T>C MANE Select	ENSP00000358532.3:p.Leu89Pro
ENST00000369519.3:c.266T>C	ENSP00000358532.3:p.Leu89Pro
NM_001134363.2:c.266T>C	NP_001127835.2:p.Leu89Pro
XM_011539697.1:c.-119T>C	XP_011537999.1:n.-119T>C
XM_017016103.2:c.101T>C	XP_016871592.1:p.Leu34Pro
XM_017016104.2:c.-119T>C	XP_016871593.1:n.-119T>C
NM_001134363.3:c.266T>C MANE Select	NP_001127835.2:p.Leu89Pro