Canonical Allele Identifier: CA14926435

Gene: CSF2RB

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36914004G>A , CM000684.2:g.36914004G>A	GRCh38
NC_000022.10:g.37310046G>A , CM000684.1:g.37310046G>A	GRCh37
NC_000022.9:g.35639992G>A	NCBI36
NG_008040.1:g.5372G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403662.8:c.-173+327G>A MANE Select	ENSP00000384053.3:n.-173+327G>A
ENST00000262825.9:c.-173+327G>A	ENSP00000262825.6:n.-173+327G>A
ENST00000403662.7:c.-173+327G>A	ENSP00000384053.3:n.-173+327G>A
NM_000395.2:c.-173+327G>A	NP_000386.1:n.-173+327G>A
XM_005261340.2:c.-173+327G>A	XP_005261397.1:n.-173+327G>A
XM_011529903.1:c.-173+327G>A	XP_011528205.1:n.-173+327G>A
XM_011529904.1:c.-173+327G>A	XP_011528206.1:n.-173+327G>A
XM_011529905.1:c.-173+327G>A	XP_011528207.1:n.-173+327G>A
XM_005261340.3:c.-173+327G>A	XP_005261397.1:n.-173+327G>A
XM_011529903.2:c.-173+327G>A	XP_011528205.1:n.-173+327G>A
XM_011529904.2:c.-173+327G>A	XP_011528206.1:n.-173+327G>A
XM_011529905.2:c.-173+327G>A	XP_011528207.1:n.-173+327G>A
NM_000395.3:c.-173+327G>A MANE Select	NP_000386.1:n.-173+327G>A