Canonical Allele Identifier: CA2404098741
Community Standard Title: NM_000395.3(CSF2RB):c.77-205T=
Gene: CSF2RB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36923039T= , CM000684.2:g.36923039T= GRCh38
NC_000022.10:g.37319081T= , CM000684.1:g.37319081T= GRCh37
NC_000022.9:g.35649027T= NCBI36
NG_008040.1:g.14407T=

Transcript Alleles

HGVS Amino-acid Change
NM_000395.3:c.77-205T= MANE Select NP_000386.1:n.77-205T=
ENST00000403662.8:c.77-205T= MANE Select ENSP00000384053.3:n.77-205T=
NM_000395.2:c.77-205T= NP_000386.1:n.77-205T=
ENST00000262825.9:c.77-205T= ENSP00000262825.6:n.77-205T=
ENST00000403662.7:c.77-205T= ENSP00000384053.3:n.77-205T=
ENST00000406230.5:c.77-205T= ENSP00000385271.1:n.77-205T=
ENST00000421539.1:c.-164-205T= ENSP00000393585.1:n.-164-205T=
XM_005261340.2:c.77-205T= XP_005261397.1:n.77-205T=
XM_005261340.3:c.77-205T= XP_005261397.1:n.77-205T=
XM_011529903.1:c.77-205T= XP_011528205.1:n.77-205T=
XM_011529903.2:c.77-205T= XP_011528205.1:n.77-205T=
XM_011529904.1:c.77-205T= XP_011528206.1:n.77-205T=
XM_011529904.2:c.77-205T= XP_011528206.1:n.77-205T=
XM_011529905.1:c.77-205T= XP_011528207.1:n.77-205T=
XM_011529905.2:c.77-205T= XP_011528207.1:n.77-205T=
XR_938230.1:n.230+2711A=