Canonical Allele Identifier: CA2610889866
Gene: RBM20 HGNC NCBI

Linked Data

gnomAD v4: 10-110644348-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110644348A>C , CM000672.2:g.110644348A>C GRCh38
NC_000010.10:g.112404106A>C , CM000672.1:g.112404106A>C GRCh37
NC_000010.9:g.112394096A>C NCBI36
NG_021177.1:g.4952A>C , LRG_382:g.4952A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369519.4:c.-107A>C MANE Select ENSP00000358532.3:n.-107A>C
XM_017016103.2:c.26+908A>C XP_016871592.1:n.26+908A>C
NM_001134363.3:c.-107A>C MANE Select NP_001127835.2:n.-107A>C
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