Canonical Allele Identifier: CA932504720
Gene: RBM20 HGNC NCBI

Linked Data

dbSNP Id: rs1861831287
gnomAD v3: 10-110644277-A-G
gnomAD v4: 10-110644277-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110644277A>G , CM000672.2:g.110644277A>G GRCh38
NC_000010.10:g.112404035A>G , CM000672.1:g.112404035A>G GRCh37
NC_000010.9:g.112394025A>G NCBI36
NG_021177.1:g.4881A>G , LRG_382:g.4881A>G

Transcript Alleles

HGVS Amino-acid Change
XM_017016103.2:c.26+837A>G XP_016871592.1:n.26+837A>G
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