Canonical Allele Identifier: CA659823690

Gene: RBM20

Linked Data

• dbSNP Id: rs1293441827
• gnomAD v3: 10-110812217-G-A
• gnomAD v4: 10-110812217-G-A
• MyVariant Identifiers: chr10:g.112571975G>A (hg19) ; chr10:g.110812217G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110812217G>A , CM000672.2:g.110812217G>A	GRCh38
NC_000010.10:g.112571975G>A , CM000672.1:g.112571975G>A	GRCh37
NC_000010.9:g.112561965G>A	NCBI36
NG_021177.1:g.172821G>A , LRG_382:g.172821G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000369519.4:c.1881-61G>A MANE Select	ENSP00000358532.3:n.1881-61G>A
ENST00000369519.3:c.1881-61G>A	ENSP00000358532.3:n.1881-61G>A
NM_001134363.2:c.1881-61G>A	NP_001127835.2:n.1881-61G>A
XM_011539697.1:c.1497-61G>A	XP_011537999.1:n.1497-61G>A
XM_017016103.2:c.1716-61G>A	XP_016871592.1:n.1716-61G>A
XM_017016104.2:c.1497-61G>A	XP_016871593.1:n.1497-61G>A
NM_001134363.3:c.1881-61G>A MANE Select	NP_001127835.2:n.1881-61G>A