Canonical Allele Identifier: CA500057022

Gene: STAT5B

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42202405C>G , CM000679.2:g.42202405C>G	GRCh38
NC_000017.10:g.40354423C>G , CM000679.1:g.40354423C>G	GRCh37
NC_000017.9:g.37607949C>G	NCBI36
NG_007271.1:g.79002G>C , LRG_192:g.79002G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415845.2:c.2172G>C	ENSP00000398379.2:p.Thr724=
ENST00000498674.2:n.704G>C
ENST00000698774.1:n.3032G>C
ENST00000698775.1:c.*2178G>C	ENSP00000513922.1:n.*2178G>C
ENST00000698776.1:c.2172G>C	ENSP00000513923.1:p.Thr724=
ENST00000698777.1:c.2172G>C	ENSP00000513924.1:p.Thr724=
ENST00000698778.1:c.2109G>C	ENSP00000513925.1:p.Thr703=
ENST00000698779.1:c.2172G>C	ENSP00000513926.1:p.Thr724=
ENST00000698801.1:n.2043G>C
ENST00000698802.1:c.1859G>C	ENSP00000513944.1:n.1859G>C
ENST00000698803.1:c.*1917G>C	ENSP00000513945.1:n.*1917G>C
ENST00000698804.1:n.4591G>C
ENST00000698805.1:n.3515G>C
ENST00000698806.1:c.*1886G>C	ENSP00000513946.1:n.*1886G>C
ENST00000698807.1:n.4234G>C
ENST00000698808.1:c.2169G>C	ENSP00000513947.1:p.Thr723=
ENST00000698809.1:c.2079G>C	ENSP00000513948.1:p.Thr693=
ENST00000698810.1:c.*1922G>C	ENSP00000513949.1:n.*1922G>C
ENST00000698811.1:n.2567G>C
ENST00000698812.1:c.*2186G>C	ENSP00000513950.1:n.*2186G>C
ENST00000698813.1:c.*203G>C	ENSP00000513951.1:n.*203G>C
ENST00000698814.1:c.*71G>C	ENSP00000513952.1:n.*71G>C
ENST00000698815.1:c.*320G>C	ENSP00000513953.1:n.*320G>C
ENST00000293328.8:c.2172G>C MANE Select	ENSP00000293328.3:p.Thr724=
ENST00000293328.7:c.2172G>C	ENSP00000293328.3:p.Thr724=
ENST00000498674.1:n.240G>C
NM_012448.3:c.2172G>C , LRG_192t1:c.2172G>C	NP_036580.2:p.Thr724=
XM_005257625.2:c.1890G>C	XP_005257682.1:p.Thr630=
XM_017024977.1:c.1890G>C	XP_016880466.1:p.Thr630=
XM_024450897.1:c.2172G>C	XP_024306665.1:p.Thr724=
XM_024450898.1:c.2172G>C	XP_024306666.1:p.Thr724=
NM_012448.4:c.2172G>C MANE Select	NP_036580.2:p.Thr724=