Canonical Allele Identifier: CA2684771326

Gene: RBM28

Linked Data

• gnomAD v4: 7-128330796-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128330796C>A , CM000669.2:g.128330796C>A	GRCh38
NC_000007.13:g.127970849C>A , CM000669.1:g.127970849C>A	GRCh37
NC_000007.12:g.127758085C>A	NCBI36
NG_015802.1:g.18114G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000223073.6:c.1129+23G>T MANE Select	ENSP00000223073.1:n.1129+23G>T
ENST00000415472.6:c.706+23G>T	ENSP00000390517.2:n.706+23G>T
ENST00000487602.5:c.546+23G>T
NM_001166135.1:c.706+23G>T	NP_001159607.1:n.706+23G>T
NM_018077.2:c.1129+23G>T	NP_060547.2:n.1129+23G>T
XM_011516370.1:c.1231+23G>T	XP_011514672.1:n.1231+23G>T
XM_011516371.1:c.135+23G>T	XP_011514673.1:n.135+23G>T
XR_927487.1:n.1351+23G>T
XM_011516370.3:c.1231+23G>T	XP_011514672.1:n.1231+23G>T
XM_017012389.1:c.1231+23G>T	XP_016867878.1:n.1231+23G>T
XM_017012390.1:c.1129+23G>T	XP_016867879.1:n.1129+23G>T
XR_001744830.1:n.1353+23G>T
NM_001166135.2:c.706+23G>T	NP_001159607.1:n.706+23G>T
NM_018077.3:c.1129+23G>T MANE Select	NP_060547.2:n.1129+23G>T