Canonical Allele Identifier: CA378379801
Gene: RBM20 HGNC NCBI

Linked Data

dbSNP Id: rs1202155519

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110780971A>G , CM000672.2:g.110780971A>G GRCh38
NC_000010.10:g.112540729A>G , CM000672.1:g.112540729A>G GRCh37
NC_000010.9:g.112530719A>G NCBI36
NG_021177.1:g.141575A>G , LRG_382:g.141575A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369519.4:c.362A>G MANE Select ENSP00000358532.3:p.Asn121Ser
ENST00000369519.3:c.362A>G ENSP00000358532.3:p.Asn121Ser
NM_001134363.2:c.362A>G NP_001127835.2:p.Asn121Ser
XM_011539697.1:c.-23A>G XP_011537999.1:n.-23A>G
XM_017016103.2:c.197A>G XP_016871592.1:p.Asn66Ser
XM_017016104.2:c.-23A>G XP_016871593.1:n.-23A>G
NM_001134363.3:c.362A>G MANE Select NP_001127835.2:p.Asn121Ser