Canonical Allele Identifier: CA14993133

Gene: CSF2RB

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36937067G>T , CM000684.2:g.36937067G>T	GRCh38
NC_000022.10:g.37333109G>T , CM000684.1:g.37333109G>T	GRCh37
NC_000022.9:g.35663055G>T	NCBI36
NG_008040.1:g.28435G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000395.3:c.1569-310G>T MANE Select	NP_000386.1:n.1569-310G>T
ENST00000403662.8:c.1569-310G>T MANE Select	ENSP00000384053.3:n.1569-310G>T
NM_000395.2:c.1569-310G>T	NP_000386.1:n.1569-310G>T
ENST00000262825.9:c.1569-310G>T	ENSP00000262825.6:n.1569-310G>T
ENST00000403662.7:c.1569-310G>T	ENSP00000384053.3:n.1569-310G>T
ENST00000406230.5:c.1587-310G>T	ENSP00000385271.1:n.1587-310G>T
XM_005261340.2:c.1587-310G>T	XP_005261397.1:n.1587-310G>T
XM_005261340.3:c.1587-310G>T	XP_005261397.1:n.1587-310G>T
XM_011529903.1:c.1623-310G>T	XP_011528205.1:n.1623-310G>T
XM_011529903.2:c.1623-310G>T	XP_011528205.1:n.1623-310G>T
XM_011529904.1:c.1605-310G>T	XP_011528206.1:n.1605-310G>T
XM_011529904.2:c.1605-310G>T	XP_011528206.1:n.1605-310G>T
XM_011529905.1:c.1519-310G>T	XP_011528207.1:n.1519-310G>T
XM_011529905.2:c.1519-310G>T	XP_011528207.1:n.1519-310G>T