Canonical Allele Identifier: CA932504784
Gene: RBM20 HGNC NCBI

Linked Data

dbSNP Id: rs1489405180
gnomAD v3: 10-110644368-G-C
gnomAD v4: 10-110644368-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110644368G>C , CM000672.2:g.110644368G>C GRCh38
NC_000010.10:g.112404126G>C , CM000672.1:g.112404126G>C GRCh37
NC_000010.9:g.112394116G>C NCBI36
NG_021177.1:g.4972G>C , LRG_382:g.4972G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369519.4:c.-87G>C MANE Select ENSP00000358532.3:n.-87G>C
XM_017016103.2:c.26+928G>C XP_016871592.1:n.26+928G>C
NM_001134363.3:c.-87G>C MANE Select NP_001127835.2:n.-87G>C
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