Canonical Allele Identifier: CA2610892745
Gene: RBM20 HGNC NCBI

Linked Data

gnomAD v4: 10-110812211-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110812211C>A , CM000672.2:g.110812211C>A GRCh38
NC_000010.10:g.112571969C>A , CM000672.1:g.112571969C>A GRCh37
NC_000010.9:g.112561959C>A NCBI36
NG_021177.1:g.172815C>A , LRG_382:g.172815C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369519.4:c.1881-67C>A MANE Select ENSP00000358532.3:n.1881-67C>A
ENST00000369519.3:c.1881-67C>A ENSP00000358532.3:n.1881-67C>A
NM_001134363.2:c.1881-67C>A NP_001127835.2:n.1881-67C>A
XM_011539697.1:c.1497-67C>A XP_011537999.1:n.1497-67C>A
XM_017016103.2:c.1716-67C>A XP_016871592.1:n.1716-67C>A
XM_017016104.2:c.1497-67C>A XP_016871593.1:n.1497-67C>A
NM_001134363.3:c.1881-67C>A MANE Select NP_001127835.2:n.1881-67C>A
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