Canonical Allele Identifier: CA378372127

Gene: RBM20

Linked Data

• gnomAD v4: 10-110812532-A-T
• MyVariant Identifiers: chr10:g.112572290A>T (hg19) ; chr10:g.110812532A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110812532A>T , CM000672.2:g.110812532A>T	GRCh38
NC_000010.10:g.112572290A>T , CM000672.1:g.112572290A>T	GRCh37
NC_000010.9:g.112562280A>T	NCBI36
NG_021177.1:g.173136A>T , LRG_382:g.173136A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369519.4:c.2135A>T MANE Select	ENSP00000358532.3:p.Lys712Ile
ENST00000369519.3:c.2135A>T	ENSP00000358532.3:p.Lys712Ile
NM_001134363.2:c.2135A>T	NP_001127835.2:p.Lys712Ile
XM_011539697.1:c.1751A>T	XP_011537999.1:p.Lys584Ile
XM_017016103.2:c.1970A>T	XP_016871592.1:p.Lys657Ile
XM_017016104.2:c.1751A>T	XP_016871593.1:p.Lys584Ile
NM_001134363.3:c.2135A>T MANE Select	NP_001127835.2:p.Lys712Ile