Canonical Allele Identifier: CA471368040
Gene: RBM20 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.112572060T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110812302T>A , CM000672.2:g.110812302T>A GRCh38
NC_000010.10:g.112572060T>A , CM000672.1:g.112572060T>A GRCh37
NC_000010.9:g.112562050T>A NCBI36
NG_021177.1:g.172906T>A , LRG_382:g.172906T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369519.4:c.1905T>A MANE Select ENSP00000358532.3:p.Ser635=
ENST00000369519.3:c.1905T>A ENSP00000358532.3:p.Ser635=
NM_001134363.2:c.1905T>A NP_001127835.2:p.Ser635=
XM_011539697.1:c.1521T>A XP_011537999.1:p.Ser507=
XM_017016103.2:c.1740T>A XP_016871592.1:p.Ser580=
XM_017016104.2:c.1521T>A XP_016871593.1:p.Ser507=
NM_001134363.3:c.1905T>A MANE Select NP_001127835.2:p.Ser635=
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