Canonical Allele Identifier: CA471368054
Gene: RBM20 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.112572078G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110812320G>C , CM000672.2:g.110812320G>C GRCh38
NC_000010.10:g.112572078G>C , CM000672.1:g.112572078G>C GRCh37
NC_000010.9:g.112562068G>C NCBI36
NG_021177.1:g.172924G>C , LRG_382:g.172924G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369519.4:c.1923G>C MANE Select ENSP00000358532.3:p.Arg641=
ENST00000369519.3:c.1923G>C ENSP00000358532.3:p.Arg641=
NM_001134363.2:c.1923G>C NP_001127835.2:p.Arg641=
XM_011539697.1:c.1539G>C XP_011537999.1:p.Arg513=
XM_017016103.2:c.1758G>C XP_016871592.1:p.Arg586=
XM_017016104.2:c.1539G>C XP_016871593.1:p.Arg513=
NM_001134363.3:c.1923G>C MANE Select NP_001127835.2:p.Arg641=