Canonical Allele Identifier: CA378527489
Gene: RBM20 HGNC NCBI

Linked Data

gnomAD v4: 10-110644519-T-C
MyVariant Identifiers: chr10:g.112404277T>C (hg19) chr10:g.110644519T>C (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000369519.4:c.65T>C MANE Select ENSP00000358532.3:p.Val22Ala
ENST00000369519.3:c.65T>C ENSP00000358532.3:p.Val22Ala
NM_001134363.2:c.65T>C NP_001127835.2:p.Val22Ala
XM_017016103.2:c.26+1079T>C XP_016871592.1:n.26+1079T>C
NM_001134363.3:c.65T>C MANE Select NP_001127835.2:p.Val22Ala
Search 100 bp 5'
Search 100 bp 3'