Canonical Allele Identifier: CA378374278
Gene: RBM20 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.112572623A>C (hg19) chr10:g.110812865A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110812865A>C , CM000672.2:g.110812865A>C GRCh38
NC_000010.10:g.112572623A>C , CM000672.1:g.112572623A>C GRCh37
NC_000010.9:g.112562613A>C NCBI36
NG_021177.1:g.173469A>C , LRG_382:g.173469A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369519.4:c.2468A>C MANE Select ENSP00000358532.3:p.Asn823Thr
ENST00000369519.3:c.2468A>C ENSP00000358532.3:p.Asn823Thr
NM_001134363.2:c.2468A>C NP_001127835.2:p.Asn823Thr
XM_011539697.1:c.2084A>C XP_011537999.1:p.Asn695Thr
XM_017016103.2:c.2303A>C XP_016871592.1:p.Asn768Thr
XM_017016104.2:c.2084A>C XP_016871593.1:p.Asn695Thr
NM_001134363.3:c.2468A>C MANE Select NP_001127835.2:p.Asn823Thr
Search 100 bp 5'
Search 100 bp 3'