Canonical Allele Identifier: CA10213590

Gene: CSF2RB

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36930468C>A , CM000684.2:g.36930468C>A	GRCh38
NC_000022.10:g.37326510C>A , CM000684.1:g.37326510C>A	GRCh37
NC_000022.9:g.35656456C>A	NCBI36
NG_008040.1:g.21836C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403662.8:c.812C>A MANE Select	ENSP00000384053.3:p.Ser271Ter
ENST00000262825.9:c.812C>A	ENSP00000262825.6:p.Ser271Ter
ENST00000403662.7:c.812C>A	ENSP00000384053.3:p.Ser271Ter
ENST00000406230.5:c.812C>A	ENSP00000385271.1:p.Ser271Ter
ENST00000421539.1:c.572C>A	ENSP00000393585.1:p.Ser191Ter
NM_000395.2:c.812C>A	NP_000386.1:p.Ser271Ter
XM_005261340.2:c.812C>A	XP_005261397.1:p.Ser271Ter
XM_011529903.1:c.812C>A	XP_011528205.1:p.Ser271Ter
XM_011529904.1:c.812C>A	XP_011528206.1:p.Ser271Ter
XM_011529905.1:c.812C>A	XP_011528207.1:p.Ser271Ter
XM_005261340.3:c.812C>A	XP_005261397.1:p.Ser271Ter
XM_011529903.2:c.812C>A	XP_011528205.1:p.Ser271Ter
XM_011529904.2:c.812C>A	XP_011528206.1:p.Ser271Ter
XM_011529905.2:c.812C>A	XP_011528207.1:p.Ser271Ter
NM_000395.3:c.812C>A MANE Select	NP_000386.1:p.Ser271Ter