Canonical Allele Identifier: CA6808323

Gene: RBM19

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.113918420C>G , CM000674.2:g.113918420C>G	GRCh38
NC_000012.11:g.114356225C>G , CM000674.1:g.114356225C>G	GRCh37
NC_000012.10:g.112840608C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_016196.4:c.2413G>C MANE Select	NP_057280.2:p.Glu805Gln
ENST00000261741.10:c.2413G>C MANE Select	ENSP00000261741.5:p.Glu805Gln
NM_001146698.1:c.2413G>C	NP_001140170.1:p.Glu805Gln
NM_001146698.2:c.2413G>C	NP_001140170.1:p.Glu805Gln
NM_001146699.1:c.2413G>C	NP_001140171.1:p.Glu805Gln
NM_001146699.2:c.2413G>C	NP_001140171.1:p.Glu805Gln
NM_016196.3:c.2413G>C	NP_057280.2:p.Glu805Gln
ENST00000261741.9:c.2413G>C	ENSP00000261741.5:p.Glu805Gln
ENST00000392561.7:c.2413G>C	ENSP00000376344.3:p.Glu805Gln
ENST00000545145.6:c.2413G>C	ENSP00000442053.2:p.Glu805Gln
ENST00000552386.1:n.547G>C
XM_011539038.1:c.2341G>C	XP_011537340.1:p.Glu781Gln
XM_017020280.1:c.2341G>C	XP_016875769.1:p.Glu781Gln
XM_017020281.1:c.2341G>C	XP_016875770.1:p.Glu781Gln
XR_001748932.1:n.2485G>C
XR_944848.1:n.2530G>C
XR_944848.2:n.2557G>C