Canonical Allele Identifier: CA378373291
Gene: RBM20 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.112572467A>C (hg19) chr10:g.110812709A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110812709A>C , CM000672.2:g.110812709A>C GRCh38
NC_000010.10:g.112572467A>C , CM000672.1:g.112572467A>C GRCh37
NC_000010.9:g.112562457A>C NCBI36
NG_021177.1:g.173313A>C , LRG_382:g.173313A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369519.4:c.2312A>C MANE Select ENSP00000358532.3:p.Tyr771Ser
ENST00000369519.3:c.2312A>C ENSP00000358532.3:p.Tyr771Ser
NM_001134363.2:c.2312A>C NP_001127835.2:p.Tyr771Ser
XM_011539697.1:c.1928A>C XP_011537999.1:p.Tyr643Ser
XM_017016103.2:c.2147A>C XP_016871592.1:p.Tyr716Ser
XM_017016104.2:c.1928A>C XP_016871593.1:p.Tyr643Ser
NM_001134363.3:c.2312A>C MANE Select NP_001127835.2:p.Tyr771Ser
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