Canonical Allele Identifier: CA378379316
Gene: RBM20 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.112540639T>C (hg19) chr10:g.110780881T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110780881T>C , CM000672.2:g.110780881T>C GRCh38
NC_000010.10:g.112540639T>C , CM000672.1:g.112540639T>C GRCh37
NC_000010.9:g.112530629T>C NCBI36
NG_021177.1:g.141485T>C , LRG_382:g.141485T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369519.4:c.272T>C MANE Select ENSP00000358532.3:p.Leu91Pro
ENST00000369519.3:c.272T>C ENSP00000358532.3:p.Leu91Pro
NM_001134363.2:c.272T>C NP_001127835.2:p.Leu91Pro
XM_011539697.1:c.-113T>C XP_011537999.1:n.-113T>C
XM_017016103.2:c.107T>C XP_016871592.1:p.Leu36Pro
XM_017016104.2:c.-113T>C XP_016871593.1:n.-113T>C
NM_001134363.3:c.272T>C MANE Select NP_001127835.2:p.Leu91Pro
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