Canonical Allele Identifier: CA378370659
Gene: RBM20 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110812375A>C , CM000672.2:g.110812375A>C GRCh38
NC_000010.10:g.112572133A>C , CM000672.1:g.112572133A>C GRCh37
NC_000010.9:g.112562123A>C NCBI36
NG_021177.1:g.172979A>C , LRG_382:g.172979A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369519.4:c.1978A>C MANE Select ENSP00000358532.3:p.Ser660Arg
ENST00000369519.3:c.1978A>C ENSP00000358532.3:p.Ser660Arg
NM_001134363.2:c.1978A>C NP_001127835.2:p.Ser660Arg
XM_011539697.1:c.1594A>C XP_011537999.1:p.Ser532Arg
XM_017016103.2:c.1813A>C XP_016871592.1:p.Ser605Arg
XM_017016104.2:c.1594A>C XP_016871593.1:p.Ser532Arg
NM_001134363.3:c.1978A>C MANE Select NP_001127835.2:p.Ser660Arg