Canonical Allele Identifier: CA2404103903
Community Standard Title: NM_000395.3(CSF2RB):c.1278C= (p.Ser426=)
Gene: CSF2RB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36933957C= , CM000684.2:g.36933957C= GRCh38
NC_000022.10:g.37329999C= , CM000684.1:g.37329999C= GRCh37
NC_000022.9:g.35659945C= NCBI36
NG_008040.1:g.25325C=

Transcript Alleles

HGVS Amino-acid Change
NM_000395.3:c.1278C= MANE Select NP_000386.1:p.Ser426=
ENST00000403662.8:c.1278C= MANE Select ENSP00000384053.3:p.Ser426=
NM_000395.2:c.1278C= NP_000386.1:p.Ser426=
ENST00000262825.9:c.1278C= ENSP00000262825.6:p.Ser426=
ENST00000403662.7:c.1278C= ENSP00000384053.3:p.Ser426=
ENST00000406230.5:c.1296C= ENSP00000385271.1:p.Ser432=
XM_005261340.2:c.1296C= XP_005261397.1:p.Ser432=
XM_005261340.3:c.1296C= XP_005261397.1:p.Ser432=
XM_011529903.1:c.1296C= XP_011528205.1:p.Ser432=
XM_011529903.2:c.1296C= XP_011528205.1:p.Ser432=
XM_011529904.1:c.1278C= XP_011528206.1:p.Ser426=
XM_011529904.2:c.1278C= XP_011528206.1:p.Ser426=
XM_011529905.1:c.1296C= XP_011528207.1:p.Ser432=
XM_011529905.2:c.1296C= XP_011528207.1:p.Ser432=