Canonical Allele Identifier: CA378379299
Gene: RBM20 HGNC NCBI

Linked Data

dbSNP Id: rs1844329199
gnomAD v3: 10-110780878-A-G
gnomAD v4: 10-110780878-A-G
MyVariant Identifiers: chr10:g.112540636A>G (hg19) chr10:g.110780878A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110780878A>G , CM000672.2:g.110780878A>G GRCh38
NC_000010.10:g.112540636A>G , CM000672.1:g.112540636A>G GRCh37
NC_000010.9:g.112530626A>G NCBI36
NG_021177.1:g.141482A>G , LRG_382:g.141482A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369519.4:c.269A>G MANE Select ENSP00000358532.3:p.Gln90Arg
ENST00000369519.3:c.269A>G ENSP00000358532.3:p.Gln90Arg
NM_001134363.2:c.269A>G NP_001127835.2:p.Gln90Arg
XM_011539697.1:c.-116A>G XP_011537999.1:n.-116A>G
XM_017016103.2:c.104A>G XP_016871592.1:p.Gln35Arg
XM_017016104.2:c.-116A>G XP_016871593.1:n.-116A>G
NM_001134363.3:c.269A>G MANE Select NP_001127835.2:p.Gln90Arg
Search 100 bp 5'
Search 100 bp 3'