Canonical Allele Identifier: CA378370756

Gene: RBM20

Linked Data

• gnomAD v4: 10-110812385-G-C
• MyVariant Identifiers: chr10:g.112572143G>C (hg19) ; chr10:g.110812385G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110812385G>C , CM000672.2:g.110812385G>C	GRCh38
NC_000010.10:g.112572143G>C , CM000672.1:g.112572143G>C	GRCh37
NC_000010.9:g.112562133G>C	NCBI36
NG_021177.1:g.172989G>C , LRG_382:g.172989G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369519.4:c.1988G>C MANE Select	ENSP00000358532.3:p.Gly663Ala
ENST00000369519.3:c.1988G>C	ENSP00000358532.3:p.Gly663Ala
NM_001134363.2:c.1988G>C	NP_001127835.2:p.Gly663Ala
XM_011539697.1:c.1604G>C	XP_011537999.1:p.Gly535Ala
XM_017016103.2:c.1823G>C	XP_016871592.1:p.Gly608Ala
XM_017016104.2:c.1604G>C	XP_016871593.1:p.Gly535Ala
NM_001134363.3:c.1988G>C MANE Select	NP_001127835.2:p.Gly663Ala