Canonical Allele Identifier: CA378370695
Gene: RBM20 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110812378C>G , CM000672.2:g.110812378C>G GRCh38
NC_000010.10:g.112572136C>G , CM000672.1:g.112572136C>G GRCh37
NC_000010.9:g.112562126C>G NCBI36
NG_021177.1:g.172982C>G , LRG_382:g.172982C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369519.4:c.1981C>G MANE Select ENSP00000358532.3:p.Pro661Ala
ENST00000369519.3:c.1981C>G ENSP00000358532.3:p.Pro661Ala
NM_001134363.2:c.1981C>G NP_001127835.2:p.Pro661Ala
XM_011539697.1:c.1597C>G XP_011537999.1:p.Pro533Ala
XM_017016103.2:c.1816C>G XP_016871592.1:p.Pro606Ala
XM_017016104.2:c.1597C>G XP_016871593.1:p.Pro533Ala
NM_001134363.3:c.1981C>G MANE Select NP_001127835.2:p.Pro661Ala