Canonical Allele Identifier: CA471368043
Gene: RBM20 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.112572063T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110812305T>A , CM000672.2:g.110812305T>A GRCh38
NC_000010.10:g.112572063T>A , CM000672.1:g.112572063T>A GRCh37
NC_000010.9:g.112562053T>A NCBI36
NG_021177.1:g.172909T>A , LRG_382:g.172909T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369519.4:c.1908T>A MANE Select ENSP00000358532.3:p.Arg636=
ENST00000369519.3:c.1908T>A ENSP00000358532.3:p.Arg636=
NM_001134363.2:c.1908T>A NP_001127835.2:p.Arg636=
XM_011539697.1:c.1524T>A XP_011537999.1:p.Arg508=
XM_017016103.2:c.1743T>A XP_016871592.1:p.Arg581=
XM_017016104.2:c.1524T>A XP_016871593.1:p.Arg508=
NM_001134363.3:c.1908T>A MANE Select NP_001127835.2:p.Arg636=
Search 100 bp 5'
Search 100 bp 3'