Canonical Allele Identifier: CA378370370
Gene: RBM20 HGNC NCBI

Linked Data

dbSNP Id: rs143785916
MyVariant Identifiers: chr10:g.112572077G>C (hg19) chr10:g.110812319G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110812319G>C , CM000672.2:g.110812319G>C GRCh38
NC_000010.10:g.112572077G>C , CM000672.1:g.112572077G>C GRCh37
NC_000010.9:g.112562067G>C NCBI36
NG_021177.1:g.172923G>C , LRG_382:g.172923G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369519.4:c.1922G>C MANE Select ENSP00000358532.3:p.Arg641Pro
ENST00000369519.3:c.1922G>C ENSP00000358532.3:p.Arg641Pro
NM_001134363.2:c.1922G>C NP_001127835.2:p.Arg641Pro
XM_011539697.1:c.1538G>C XP_011537999.1:p.Arg513Pro
XM_017016103.2:c.1757G>C XP_016871592.1:p.Arg586Pro
XM_017016104.2:c.1538G>C XP_016871593.1:p.Arg513Pro
NM_001134363.3:c.1922G>C MANE Select NP_001127835.2:p.Arg641Pro
Search 100 bp 5'
Search 100 bp 3'