Canonical Allele Identifier: CA133295
Gene: RBM20 HGNC NCBI

Linked Data

ClinVar Variation Id: 43983
ClinVar RCV Id: RCV000036958 RCV000475115 RCV000621531 RCV000769268 RCV001705665
dbSNP Id: rs41292592
ExAC: 10:112572147 C / T
gnomAD v2: 10-112572147-C-T
gnomAD v3: 10-110812389-C-T
gnomAD v4: 10-110812389-C-T
MyVariant Identifiers: chr10:g.112572147C>T (hg19) chr10:g.110812389C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110812389C>T , CM000672.2:g.110812389C>T GRCh38
NC_000010.10:g.112572147C>T , CM000672.1:g.112572147C>T GRCh37
NC_000010.9:g.112562137C>T NCBI36
NG_021177.1:g.172993C>T , LRG_382:g.172993C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369519.4:c.1992C>T MANE Select ENSP00000358532.3:p.Pro664=
ENST00000369519.3:c.1992C>T ENSP00000358532.3:p.Pro664=
NM_001134363.2:c.1992C>T NP_001127835.2:p.Pro664=
XM_011539697.1:c.1608C>T XP_011537999.1:p.Pro536=
XM_017016103.2:c.1827C>T XP_016871592.1:p.Pro609=
XM_017016104.2:c.1608C>T XP_016871593.1:p.Pro536=
NM_001134363.3:c.1992C>T MANE Select NP_001127835.2:p.Pro664=
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