Canonical Allele Identifier: CA2610892698
Gene: RBM20 HGNC NCBI

Linked Data

gnomAD v4: 10-110812168-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110812168A>T , CM000672.2:g.110812168A>T GRCh38
NC_000010.10:g.112571926A>T , CM000672.1:g.112571926A>T GRCh37
NC_000010.9:g.112561916A>T NCBI36
NG_021177.1:g.172772A>T , LRG_382:g.172772A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369519.4:c.1881-110A>T MANE Select ENSP00000358532.3:n.1881-110A>T
ENST00000369519.3:c.1881-110A>T ENSP00000358532.3:n.1881-110A>T
NM_001134363.2:c.1881-110A>T NP_001127835.2:n.1881-110A>T
XM_011539697.1:c.1497-110A>T XP_011537999.1:n.1497-110A>T
XM_017016103.2:c.1716-110A>T XP_016871592.1:n.1716-110A>T
XM_017016104.2:c.1497-110A>T XP_016871593.1:n.1497-110A>T
NM_001134363.3:c.1881-110A>T MANE Select NP_001127835.2:n.1881-110A>T
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