Canonical Allele Identifier: CA378371773
Gene: RBM20 HGNC NCBI

Linked Data

dbSNP Id: rs1266130657

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110812501G>T , CM000672.2:g.110812501G>T GRCh38
NC_000010.10:g.112572259G>T , CM000672.1:g.112572259G>T GRCh37
NC_000010.9:g.112562249G>T NCBI36
NG_021177.1:g.173105G>T , LRG_382:g.173105G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369519.4:c.2104G>T MANE Select ENSP00000358532.3:p.Asp702Tyr
ENST00000369519.3:c.2104G>T ENSP00000358532.3:p.Asp702Tyr
NM_001134363.2:c.2104G>T NP_001127835.2:p.Asp702Tyr
XM_011539697.1:c.1720G>T XP_011537999.1:p.Asp574Tyr
XM_017016103.2:c.1939G>T XP_016871592.1:p.Asp647Tyr
XM_017016104.2:c.1720G>T XP_016871593.1:p.Asp574Tyr
NM_001134363.3:c.2104G>T MANE Select NP_001127835.2:p.Asp702Tyr