Canonical Allele Identifier: CA2610889881
Gene: RBM20 HGNC NCBI

Linked Data

dbSNP Id: rs1861833914
gnomAD v4: 10-110644355-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110644355G>T , CM000672.2:g.110644355G>T GRCh38
NC_000010.10:g.112404113G>T , CM000672.1:g.112404113G>T GRCh37
NC_000010.9:g.112394103G>T NCBI36
NG_021177.1:g.4959G>T , LRG_382:g.4959G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369519.4:c.-100G>T MANE Select ENSP00000358532.3:n.-100G>T
XM_017016103.2:c.26+915G>T XP_016871592.1:n.26+915G>T
NM_001134363.3:c.-100G>T MANE Select NP_001127835.2:n.-100G>T
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