Canonical Allele Identifier: CA378371558
Gene: RBM20 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110812487G>C , CM000672.2:g.110812487G>C GRCh38
NC_000010.10:g.112572245G>C , CM000672.1:g.112572245G>C GRCh37
NC_000010.9:g.112562235G>C NCBI36
NG_021177.1:g.173091G>C , LRG_382:g.173091G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369519.4:c.2090G>C MANE Select ENSP00000358532.3:p.Gly697Ala
ENST00000369519.3:c.2090G>C ENSP00000358532.3:p.Gly697Ala
NM_001134363.2:c.2090G>C NP_001127835.2:p.Gly697Ala
XM_011539697.1:c.1706G>C XP_011537999.1:p.Gly569Ala
XM_017016103.2:c.1925G>C XP_016871592.1:p.Gly642Ala
XM_017016104.2:c.1706G>C XP_016871593.1:p.Gly569Ala
NM_001134363.3:c.2090G>C MANE Select NP_001127835.2:p.Gly697Ala