Canonical Allele Identifier: CA14951216
Gene: CSF2RB HGNC NCBI

Linked Data

ClinVar Variation Id: 1276886
ClinVar RCV Id: RCV001690191
dbSNP Id: rs11705394

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36933634T>C , CM000684.2:g.36933634T>C GRCh38
NC_000022.10:g.37329676T>C , CM000684.1:g.37329676T>C GRCh37
NC_000022.9:g.35659622T>C NCBI36
NG_008040.1:g.25002T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000403662.8:c.1153-198T>C MANE Select ENSP00000384053.3:n.1153-198T>C
ENST00000262825.9:c.1153-198T>C ENSP00000262825.6:n.1153-198T>C
ENST00000403662.7:c.1153-198T>C ENSP00000384053.3:n.1153-198T>C
ENST00000406230.5:c.1171-198T>C ENSP00000385271.1:n.1171-198T>C
NM_000395.2:c.1153-198T>C NP_000386.1:n.1153-198T>C
XM_005261340.2:c.1171-198T>C XP_005261397.1:n.1171-198T>C
XM_011529903.1:c.1171-198T>C XP_011528205.1:n.1171-198T>C
XM_011529904.1:c.1153-198T>C XP_011528206.1:n.1153-198T>C
XM_011529905.1:c.1171-198T>C XP_011528207.1:n.1171-198T>C
XM_005261340.3:c.1171-198T>C XP_005261397.1:n.1171-198T>C
XM_011529903.2:c.1171-198T>C XP_011528205.1:n.1171-198T>C
XM_011529904.2:c.1153-198T>C XP_011528206.1:n.1153-198T>C
XM_011529905.2:c.1171-198T>C XP_011528207.1:n.1171-198T>C
NM_000395.3:c.1153-198T>C MANE Select NP_000386.1:n.1153-198T>C