Canonical Allele Identifier: CA471464267
Gene: RBM20 HGNC NCBI

Linked Data

gnomAD v4: 10-110644610-C-T
MyVariant Identifiers: chr10:g.112404368C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110644610C>T , CM000672.2:g.110644610C>T GRCh38
NC_000010.10:g.112404368C>T , CM000672.1:g.112404368C>T GRCh37
NC_000010.9:g.112394358C>T NCBI36
NG_021177.1:g.5214C>T , LRG_382:g.5214C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369519.4:c.156C>T MANE Select ENSP00000358532.3:p.Pro52=
ENST00000369519.3:c.156C>T ENSP00000358532.3:p.Pro52=
NM_001134363.2:c.156C>T NP_001127835.2:p.Pro52=
XM_017016103.2:c.26+1170C>T XP_016871592.1:n.26+1170C>T
NM_001134363.3:c.156C>T MANE Select NP_001127835.2:p.Pro52=
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