Canonical Allele Identifier: CA471506594
Gene: RBM20 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.112540838A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110781080A>T , CM000672.2:g.110781080A>T GRCh38
NC_000010.10:g.112540838A>T , CM000672.1:g.112540838A>T GRCh37
NC_000010.9:g.112530828A>T NCBI36
NG_021177.1:g.141684A>T , LRG_382:g.141684A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369519.4:c.471A>T MANE Select ENSP00000358532.3:p.Ala157=
ENST00000369519.3:c.471A>T ENSP00000358532.3:p.Ala157=
NM_001134363.2:c.471A>T NP_001127835.2:p.Ala157=
XM_011539697.1:c.87A>T XP_011537999.1:p.Ala29=
XM_017016103.2:c.306A>T XP_016871592.1:p.Ala102=
XM_017016104.2:c.87A>T XP_016871593.1:p.Ala29=
NM_001134363.3:c.471A>T MANE Select NP_001127835.2:p.Ala157=