Canonical Allele Identifier: CA596021823
Gene: RBM20 HGNC NCBI

Linked Data

dbSNP Id: rs1402187068
gnomAD v2: 10-112404064-C-T
gnomAD v3: 10-110644306-C-T
gnomAD v4: 10-110644306-C-T
MyVariant Identifiers: chr10:g.112404064C>T (hg19) chr10:g.110644306C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110644306C>T , CM000672.2:g.110644306C>T GRCh38
NC_000010.10:g.112404064C>T , CM000672.1:g.112404064C>T GRCh37
NC_000010.9:g.112394054C>T NCBI36
NG_021177.1:g.4910C>T , LRG_382:g.4910C>T

Transcript Alleles

HGVS Amino-acid Change
XM_017016103.2:c.26+866C>T XP_016871592.1:n.26+866C>T
Search 100 bp 5'
Search 100 bp 3'