Canonical Allele Identifier: CA659845280
Gene: RBM20 HGNC NCBI

Linked Data

dbSNP Id: rs945791802
gnomAD v3: 10-110644323-G-A
gnomAD v4: 10-110644323-G-A
MyVariant Identifiers: chr10:g.112404081G>A (hg19) chr10:g.110644323G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110644323G>A , CM000672.2:g.110644323G>A GRCh38
NC_000010.10:g.112404081G>A , CM000672.1:g.112404081G>A GRCh37
NC_000010.9:g.112394071G>A NCBI36
NG_021177.1:g.4927G>A , LRG_382:g.4927G>A

Transcript Alleles

HGVS Amino-acid Change
XM_017016103.2:c.26+883G>A XP_016871592.1:n.26+883G>A
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