Canonical Allele Identifier: CA2684771339

Gene: RBM28

Linked Data

• gnomAD v4: 7-128330804-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128330804G>T , CM000669.2:g.128330804G>T	GRCh38
NC_000007.13:g.127970857G>T , CM000669.1:g.127970857G>T	GRCh37
NC_000007.12:g.127758093G>T	NCBI36
NG_015802.1:g.18106C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000223073.6:c.1129+15C>A MANE Select	ENSP00000223073.1:n.1129+15C>A
ENST00000415472.6:c.706+15C>A	ENSP00000390517.2:n.706+15C>A
ENST00000487602.5:c.546+15C>A
NM_001166135.1:c.706+15C>A	NP_001159607.1:n.706+15C>A
NM_018077.2:c.1129+15C>A	NP_060547.2:n.1129+15C>A
XM_011516370.1:c.1231+15C>A	XP_011514672.1:n.1231+15C>A
XM_011516371.1:c.135+15C>A	XP_011514673.1:n.135+15C>A
XR_927487.1:n.1351+15C>A
XM_011516370.3:c.1231+15C>A	XP_011514672.1:n.1231+15C>A
XM_017012389.1:c.1231+15C>A	XP_016867878.1:n.1231+15C>A
XM_017012390.1:c.1129+15C>A	XP_016867879.1:n.1129+15C>A
XR_001744830.1:n.1353+15C>A
NM_001166135.2:c.706+15C>A	NP_001159607.1:n.706+15C>A
NM_018077.3:c.1129+15C>A MANE Select	NP_060547.2:n.1129+15C>A