Canonical Allele Identifier: CA2610892752
Gene: RBM20 HGNC NCBI

Linked Data

gnomAD v4: 10-110812217-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110812217G>C , CM000672.2:g.110812217G>C GRCh38
NC_000010.10:g.112571975G>C , CM000672.1:g.112571975G>C GRCh37
NC_000010.9:g.112561965G>C NCBI36
NG_021177.1:g.172821G>C , LRG_382:g.172821G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369519.4:c.1881-61G>C MANE Select ENSP00000358532.3:n.1881-61G>C
ENST00000369519.3:c.1881-61G>C ENSP00000358532.3:n.1881-61G>C
NM_001134363.2:c.1881-61G>C NP_001127835.2:n.1881-61G>C
XM_011539697.1:c.1497-61G>C XP_011537999.1:n.1497-61G>C
XM_017016103.2:c.1716-61G>C XP_016871592.1:n.1716-61G>C
XM_017016104.2:c.1497-61G>C XP_016871593.1:n.1497-61G>C
NM_001134363.3:c.1881-61G>C MANE Select NP_001127835.2:n.1881-61G>C
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