Canonical Allele Identifier: CA752872966

Gene: CSF2RB

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36927946C>G , CM000684.2:g.36927946C>G	GRCh38
NC_000022.10:g.37323988C>G , CM000684.1:g.37323988C>G	GRCh37
NC_000022.9:g.35653934C>G	NCBI36
NG_008040.1:g.19314C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403662.8:c.392-1456C>G MANE Select	ENSP00000384053.3:n.392-1456C>G
ENST00000262825.9:c.392-1456C>G	ENSP00000262825.6:n.392-1456C>G
ENST00000403662.7:c.392-1456C>G	ENSP00000384053.3:n.392-1456C>G
ENST00000406230.5:c.392-1456C>G	ENSP00000385271.1:n.392-1456C>G
ENST00000421539.1:c.152-1456C>G	ENSP00000393585.1:n.152-1456C>G
NM_000395.2:c.392-1456C>G	NP_000386.1:n.392-1456C>G
XM_005261340.2:c.392-1456C>G	XP_005261397.1:n.392-1456C>G
XM_011529903.1:c.392-1456C>G	XP_011528205.1:n.392-1456C>G
XM_011529904.1:c.392-1456C>G	XP_011528206.1:n.392-1456C>G
XM_011529905.1:c.392-1456C>G	XP_011528207.1:n.392-1456C>G
XM_005261340.3:c.392-1456C>G	XP_005261397.1:n.392-1456C>G
XM_011529903.2:c.392-1456C>G	XP_011528205.1:n.392-1456C>G
XM_011529904.2:c.392-1456C>G	XP_011528206.1:n.392-1456C>G
XM_011529905.2:c.392-1456C>G	XP_011528207.1:n.392-1456C>G
NM_000395.3:c.392-1456C>G MANE Select	NP_000386.1:n.392-1456C>G