Canonical Allele Identifier: CA182859

Gene: CSF2RA

Linked Data

• dbSNP Id: rs73618036

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.1290424G>A , CM000686.2:g.1290424G>A	GRCh38
NC_000024.9:g.1359317G>A , CM000686.1:g.1359317G>A	GRCh37
NC_000024.8:g.1369317G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000711129.1:c.561G>A	ENSP00000518635.1:p.Thr187=
ENST00000711130.1:c.561G>A	ENSP00000518634.1:p.Thr187=
ENST00000711131.1:c.561G>A	ENSP00000518633.1:p.Thr187=
ENST00000711135.1:c.*644G>A	ENSP00000518636.1:n.*644G>A
ENST00000711136.1:n.598G>A
ENST00000711137.1:c.561G>A	ENSP00000518637.1:p.Thr187=
ENST00000711138.1:c.561G>A	ENSP00000518638.1:p.Thr187=
ENST00000711220.1:c.561G>A	ENSP00000518632.1:p.Thr187=
ENST00000711221.1:c.244+3226G>A	ENSP00000518631.1:n.244+3226G>A
ENST00000711223.1:c.561G>A	ENSP00000518630.1:p.Thr187=
ENST00000711224.1:c.561G>A	ENSP00000518629.1:p.Thr187=
ENST00000711225.1:c.561G>A	ENSP00000518628.1:p.Thr187=
ENST00000711226.1:c.561G>A	ENSP00000518627.1:p.Thr187=
XM_011545618.1:c.561G>A	XP_011543920.1:p.Thr187=
XM_011545619.1:c.561G>A	XP_011543921.1:p.Thr187=
XM_011545620.1:c.561G>A	XP_011543922.1:p.Thr187=
XM_011545621.1:c.561G>A	XP_011543923.1:p.Thr187=
XM_011545622.1:c.561G>A	XP_011543924.1:p.Thr187=
XM_011545623.1:c.561G>A	XP_011543925.1:p.Thr187=
XM_011545624.1:c.561G>A	XP_011543926.1:p.Thr187=
XM_011545625.1:c.561G>A	XP_011543927.1:p.Thr187=
XM_011545626.1:c.561G>A	XP_011543928.1:p.Thr187=
XM_011545627.1:c.561G>A	XP_011543929.1:p.Thr187=
XM_011545628.1:c.561G>A	XP_011543930.1:p.Thr187=
XM_011545629.1:c.429G>A	XP_011543931.1:p.Thr143=
XM_011545618.3:c.561G>A	XP_011543920.1:p.Thr187=
XM_011545620.2:c.561G>A	XP_011543922.1:p.Thr187=
XM_011545621.2:c.561G>A	XP_011543923.1:p.Thr187=
XM_011545623.3:c.561G>A	XP_011543925.1:p.Thr187=
XM_011545627.3:c.561G>A	XP_011543929.1:p.Thr187=
XM_011545628.2:c.561G>A	XP_011543930.1:p.Thr187=
XM_017030028.1:c.561G>A	XP_016885517.1:p.Thr187=
XM_017030029.1:c.561G>A	XP_016885518.1:p.Thr187=