Canonical Allele Identifier: CA378527491
Gene: RBM20 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.112404277T>G (hg19) chr10:g.110644519T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110644519T>G , CM000672.2:g.110644519T>G GRCh38
NC_000010.10:g.112404277T>G , CM000672.1:g.112404277T>G GRCh37
NC_000010.9:g.112394267T>G NCBI36
NG_021177.1:g.5123T>G , LRG_382:g.5123T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369519.4:c.65T>G MANE Select ENSP00000358532.3:p.Val22Gly
ENST00000369519.3:c.65T>G ENSP00000358532.3:p.Val22Gly
NM_001134363.2:c.65T>G NP_001127835.2:p.Val22Gly
XM_017016103.2:c.26+1079T>G XP_016871592.1:n.26+1079T>G
NM_001134363.3:c.65T>G MANE Select NP_001127835.2:p.Val22Gly
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