Canonical Allele Identifier: CA457527012

Gene: RBM28

Linked Data

• MyVariant Identifiers: chr7:g.127970876A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128330823A>C , CM000669.2:g.128330823A>C	GRCh38
NC_000007.13:g.127970876A>C , CM000669.1:g.127970876A>C	GRCh37
NC_000007.12:g.127758112A>C	NCBI36
NG_015802.1:g.18087T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000223073.6:c.1125T>G MANE Select	ENSP00000223073.1:p.Ser375=
ENST00000415472.6:c.702T>G	ENSP00000390517.2:p.Ser234=
ENST00000487602.5:c.542T>G
NM_001166135.1:c.702T>G	NP_001159607.1:p.Ser234=
NM_018077.2:c.1125T>G	NP_060547.2:p.Ser375=
XM_011516370.1:c.1227T>G	XP_011514672.1:p.Ser409=
XM_011516371.1:c.131T>G	XP_011514673.1:p.Leu44Arg
XR_927487.1:n.1347T>G
XM_011516370.3:c.1227T>G	XP_011514672.1:p.Ser409=
XM_017012389.1:c.1227T>G	XP_016867878.1:p.Ser409=
XM_017012390.1:c.1125T>G	XP_016867879.1:p.Ser375=
XR_001744830.1:n.1349T>G
NM_001166135.2:c.702T>G	NP_001159607.1:p.Ser234=
NM_018077.3:c.1125T>G MANE Select	NP_060547.2:p.Ser375=