Canonical Allele Identifier: CA906147157

Gene: IL5RA

Linked Data

• dbSNP Id: rs979560754
• MyVariant Identifiers: chr3:g.3142230C>G (hg19) ; chr3:g.3100546C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.3100546C>G , CM000665.2:g.3100546C>G	GRCh38
NC_000003.11:g.3142230C>G , CM000665.1:g.3142230C>G	GRCh37
NC_000003.10:g.3117230C>G	NCBI36
NG_029547.1:g.14829G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446632.7:c.367+1146G>C MANE Select	ENSP00000412209.2:n.367+1146G>C
ENST00000256452.7:c.367+1146G>C	ENSP00000256452.3:n.367+1146G>C
ENST00000311981.12:c.367+1146G>C	ENSP00000309196.8:n.367+1146G>C
ENST00000383846.5:c.367+1146G>C	ENSP00000373358.1:n.367+1146G>C
ENST00000418488.6:c.367+1146G>C	ENSP00000388858.2:n.367+1146G>C
ENST00000430514.6:c.367+1146G>C	ENSP00000400400.2:n.367+1146G>C
ENST00000438560.5:c.367+1146G>C	ENSP00000390753.1:n.367+1146G>C
ENST00000445701.5:c.367+1146G>C	ENSP00000398117.1:n.367+1146G>C
ENST00000446632.6:c.367+1146G>C	ENSP00000412209.2:n.367+1146G>C
ENST00000456302.5:c.367+1146G>C	ENSP00000392059.1:n.367+1146G>C
NM_000564.4:c.367+1146G>C	NP_000555.2:n.367+1146G>C
NM_001243099.1:c.367+1146G>C	NP_001230028.1:n.367+1146G>C
NM_175724.2:c.367+1146G>C	NP_783851.1:n.367+1146G>C
NM_175725.2:c.367+1146G>C	NP_783852.1:n.367+1146G>C
NM_175726.3:c.367+1146G>C	NP_783853.1:n.367+1146G>C
NM_175727.2:c.367+1146G>C	NP_783854.1:n.367+1146G>C
NM_175728.2:c.367+1146G>C	NP_783855.1:n.367+1146G>C
XM_011533677.1:c.367+1146G>C	XP_011531979.1:n.367+1146G>C
XM_011533678.1:c.367+1146G>C	XP_011531980.1:n.367+1146G>C
XM_011533679.1:c.367+1146G>C	XP_011531981.1:n.367+1146G>C
XM_011533677.2:c.367+1146G>C	XP_011531979.1:n.367+1146G>C
XM_011533678.2:c.367+1146G>C	XP_011531980.1:n.367+1146G>C
NM_000564.5:c.367+1146G>C	NP_000555.2:n.367+1146G>C
NM_001243099.2:c.367+1146G>C	NP_001230028.1:n.367+1146G>C
NM_175725.3:c.367+1146G>C	NP_783852.1:n.367+1146G>C
NM_175726.4:c.367+1146G>C MANE Select	NP_783853.1:n.367+1146G>C
NM_175728.3:c.367+1146G>C	NP_783855.1:n.367+1146G>C