Canonical Allele Identifier: CA213903175
Gene: RBM20 HGNC NCBI

Linked Data

dbSNP Id: rs998091359
MyVariant Identifiers: chr10:g.112404108G>A (hg19) chr10:g.110644350G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110644350G>A , CM000672.2:g.110644350G>A GRCh38
NC_000010.10:g.112404108G>A , CM000672.1:g.112404108G>A GRCh37
NC_000010.9:g.112394098G>A NCBI36
NG_021177.1:g.4954G>A , LRG_382:g.4954G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369519.4:c.-105G>A MANE Select ENSP00000358532.3:n.-105G>A
XM_017016103.2:c.26+910G>A XP_016871592.1:n.26+910G>A
NM_001134363.3:c.-105G>A MANE Select NP_001127835.2:n.-105G>A
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