Canonical Allele Identifier: CA6808265

Gene: RBM19

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.113915017C>T , CM000674.2:g.113915017C>T	GRCh38
NC_000012.11:g.114352822C>T , CM000674.1:g.114352822C>T	GRCh37
NC_000012.10:g.112837205C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_016196.4:c.2510G>A MANE Select	NP_057280.2:p.Arg837Gln
ENST00000261741.10:c.2510G>A MANE Select	ENSP00000261741.5:p.Arg837Gln
NM_001146698.1:c.2510G>A	NP_001140170.1:p.Arg837Gln
NM_001146698.2:c.2510G>A	NP_001140170.1:p.Arg837Gln
NM_001146699.1:c.2510G>A	NP_001140171.1:p.Arg837Gln
NM_001146699.2:c.2510G>A	NP_001140171.1:p.Arg837Gln
NM_016196.3:c.2510G>A	NP_057280.2:p.Arg837Gln
ENST00000261741.9:c.2510G>A	ENSP00000261741.5:p.Arg837Gln
ENST00000392561.7:c.2510G>A	ENSP00000376344.3:p.Arg837Gln
ENST00000545145.6:c.2510G>A	ENSP00000442053.2:p.Arg837Gln
ENST00000552386.1:n.644G>A
XM_011539038.1:c.2438G>A	XP_011537340.1:p.Arg813Gln
XM_017020280.1:c.2438G>A	XP_016875769.1:p.Arg813Gln
XM_017020281.1:c.2438G>A	XP_016875770.1:p.Arg813Gln
XR_001748932.1:n.2582G>A
XR_944848.1:n.2627G>A
XR_944848.2:n.2654G>A