Canonical Allele Identifier: CA471368096
Gene: RBM20 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.112572138T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110812380T>C , CM000672.2:g.110812380T>C GRCh38
NC_000010.10:g.112572138T>C , CM000672.1:g.112572138T>C GRCh37
NC_000010.9:g.112562128T>C NCBI36
NG_021177.1:g.172984T>C , LRG_382:g.172984T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369519.4:c.1983T>C MANE Select ENSP00000358532.3:p.Pro661=
ENST00000369519.3:c.1983T>C ENSP00000358532.3:p.Pro661=
NM_001134363.2:c.1983T>C NP_001127835.2:p.Pro661=
XM_011539697.1:c.1599T>C XP_011537999.1:p.Pro533=
XM_017016103.2:c.1818T>C XP_016871592.1:p.Pro606=
XM_017016104.2:c.1599T>C XP_016871593.1:p.Pro533=
NM_001134363.3:c.1983T>C MANE Select NP_001127835.2:p.Pro661=
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