Canonical Allele Identifier: CA2404099838

Gene: CSF2RB

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36925038T= , CM000684.2:g.36925038T=	GRCh38
NC_000022.10:g.37321080T= , CM000684.1:g.37321080T=	GRCh37
NC_000022.9:g.35651026T=	NCBI36
NG_008040.1:g.16406T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000395.3:c.201-949T= MANE Select	NP_000386.1:n.201-949T=
ENST00000403662.8:c.201-949T= MANE Select	ENSP00000384053.3:n.201-949T=
NM_000395.2:c.201-949T=	NP_000386.1:n.201-949T=
ENST00000262825.9:c.201-949T=	ENSP00000262825.6:n.201-949T=
ENST00000403662.7:c.201-949T=	ENSP00000384053.3:n.201-949T=
ENST00000406230.5:c.201-949T=	ENSP00000385271.1:n.201-949T=
ENST00000421539.1:c.-40-949T=	ENSP00000393585.1:n.-40-949T=
XM_005261340.2:c.201-949T=	XP_005261397.1:n.201-949T=
XM_005261340.3:c.201-949T=	XP_005261397.1:n.201-949T=
XM_011529903.1:c.201-949T=	XP_011528205.1:n.201-949T=
XM_011529903.2:c.201-949T=	XP_011528205.1:n.201-949T=
XM_011529904.1:c.201-949T=	XP_011528206.1:n.201-949T=
XM_011529904.2:c.201-949T=	XP_011528206.1:n.201-949T=
XM_011529905.1:c.201-949T=	XP_011528207.1:n.201-949T=
XM_011529905.2:c.201-949T=	XP_011528207.1:n.201-949T=
XR_938230.1:n.230+712A=