Canonical Allele Identifier: CA659845293
Gene: RBM20 HGNC NCBI

Linked Data

dbSNP Id: rs1416241631
gnomAD v3: 10-110644366-A-G
gnomAD v4: 10-110644366-A-G
MyVariant Identifiers: chr10:g.112404124A>G (hg19) chr10:g.110644366A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110644366A>G , CM000672.2:g.110644366A>G GRCh38
NC_000010.10:g.112404124A>G , CM000672.1:g.112404124A>G GRCh37
NC_000010.9:g.112394114A>G NCBI36
NG_021177.1:g.4970A>G , LRG_382:g.4970A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369519.4:c.-89A>G MANE Select ENSP00000358532.3:n.-89A>G
XM_017016103.2:c.26+926A>G XP_016871592.1:n.26+926A>G
NM_001134363.3:c.-89A>G MANE Select NP_001127835.2:n.-89A>G
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