Canonical Allele Identifier: CA378379783
Gene: RBM20 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110780970A>C , CM000672.2:g.110780970A>C GRCh38
NC_000010.10:g.112540728A>C , CM000672.1:g.112540728A>C GRCh37
NC_000010.9:g.112530718A>C NCBI36
NG_021177.1:g.141574A>C , LRG_382:g.141574A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369519.4:c.361A>C MANE Select ENSP00000358532.3:p.Asn121His
ENST00000369519.3:c.361A>C ENSP00000358532.3:p.Asn121His
NM_001134363.2:c.361A>C NP_001127835.2:p.Asn121His
XM_011539697.1:c.-24A>C XP_011537999.1:n.-24A>C
XM_017016103.2:c.196A>C XP_016871592.1:p.Asn66His
XM_017016104.2:c.-24A>C XP_016871593.1:n.-24A>C
NM_001134363.3:c.361A>C MANE Select NP_001127835.2:p.Asn121His