Canonical Allele Identifier: CA471464147
Gene: RBM20 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.112404218G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110644460G>C , CM000672.2:g.110644460G>C GRCh38
NC_000010.10:g.112404218G>C , CM000672.1:g.112404218G>C GRCh37
NC_000010.9:g.112394208G>C NCBI36
NG_021177.1:g.5064G>C , LRG_382:g.5064G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369519.4:c.6G>C MANE Select ENSP00000358532.3:p.Val2=
ENST00000369519.3:c.6G>C ENSP00000358532.3:p.Val2=
NM_001134363.2:c.6G>C NP_001127835.2:p.Val2=
XM_017016103.2:c.26+1020G>C XP_016871592.1:n.26+1020G>C
NM_001134363.3:c.6G>C MANE Select NP_001127835.2:p.Val2=
Search 100 bp 5'
Search 100 bp 3'