Canonical Allele Identifier: CA500214966

Gene: STAT5B

Linked Data

• MyVariant Identifiers: chr17:g.40362211G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42210193G>T , CM000679.2:g.42210193G>T	GRCh38
NC_000017.10:g.40362211G>T , CM000679.1:g.40362211G>T	GRCh37
NC_000017.9:g.37615737G>T	NCBI36
NG_007271.1:g.71214C>A , LRG_192:g.71214C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000415845.2:c.1884C>A	ENSP00000398379.2:p.Thr628=
ENST00000698774.1:n.2744C>A
ENST00000698775.1:c.*1890C>A	ENSP00000513922.1:n.*1890C>A
ENST00000698776.1:c.1884C>A	ENSP00000513923.1:p.Thr628=
ENST00000698777.1:c.1884C>A	ENSP00000513924.1:p.Thr628=
ENST00000698778.1:c.1884C>A	ENSP00000513925.1:p.Thr628=
ENST00000698779.1:c.1884C>A	ENSP00000513926.1:p.Thr628=
ENST00000698801.1:n.1755C>A
ENST00000698802.1:c.1571C>A	ENSP00000513944.1:n.1571C>A
ENST00000698803.1:c.*1629C>A	ENSP00000513945.1:n.*1629C>A
ENST00000698804.1:n.4303C>A
ENST00000698805.1:n.3227C>A
ENST00000698806.1:c.*1598C>A	ENSP00000513946.1:n.*1598C>A
ENST00000698807.1:n.3946C>A
ENST00000698808.1:c.1881C>A	ENSP00000513947.1:p.Thr627=
ENST00000698809.1:c.1791C>A	ENSP00000513948.1:p.Thr597=
ENST00000698810.1:c.*1634C>A	ENSP00000513949.1:n.*1634C>A
ENST00000698812.1:c.*1890C>A	ENSP00000513950.1:n.*1890C>A
ENST00000698813.1:c.1884C>A	ENSP00000513951.1:p.Thr628=
ENST00000698814.1:c.1884C>A	ENSP00000513952.1:p.Thr628=
ENST00000698815.1:c.*54+152C>A	ENSP00000513953.1:n.*54+152C>A
ENST00000293328.8:c.1884C>A MANE Select	ENSP00000293328.3:p.Thr628=
ENST00000293328.7:c.1884C>A	ENSP00000293328.3:p.Thr628=
ENST00000468496.5:n.728C>A
ENST00000481253.2:n.299C>A
NM_012448.3:c.1884C>A , LRG_192t1:c.1884C>A	NP_036580.2:p.Thr628=
XM_005257625.2:c.1602C>A	XP_005257682.1:p.Thr534=
XM_017024977.1:c.1602C>A	XP_016880466.1:p.Thr534=
XM_024450897.1:c.1884C>A	XP_024306665.1:p.Thr628=
XM_024450898.1:c.1884C>A	XP_024306666.1:p.Thr628=
NM_012448.4:c.1884C>A MANE Select	NP_036580.2:p.Thr628=