Canonical Allele Identifier: CA2610889872
Gene: RBM20 HGNC NCBI

Linked Data

gnomAD v4: 10-110644353-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110644353A>C , CM000672.2:g.110644353A>C GRCh38
NC_000010.10:g.112404111A>C , CM000672.1:g.112404111A>C GRCh37
NC_000010.9:g.112394101A>C NCBI36
NG_021177.1:g.4957A>C , LRG_382:g.4957A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369519.4:c.-102A>C MANE Select ENSP00000358532.3:n.-102A>C
XM_017016103.2:c.26+913A>C XP_016871592.1:n.26+913A>C
NM_001134363.3:c.-102A>C MANE Select NP_001127835.2:n.-102A>C
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