Canonical Allele Identifier: CA399576662

Gene: STAT5B

Linked Data

• MyVariant Identifiers: chr17:g.40362218C>T (hg19) ; chr17:g.42210200C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42210200C>T , CM000679.2:g.42210200C>T	GRCh38
NC_000017.10:g.40362218C>T , CM000679.1:g.40362218C>T	GRCh37
NC_000017.9:g.37615744C>T	NCBI36
NG_007271.1:g.71207G>A , LRG_192:g.71207G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000415845.2:c.1877G>A	ENSP00000398379.2:p.Gly626Asp
ENST00000698774.1:n.2737G>A
ENST00000698775.1:c.*1883G>A	ENSP00000513922.1:n.*1883G>A
ENST00000698776.1:c.1877G>A	ENSP00000513923.1:p.Gly626Asp
ENST00000698777.1:c.1877G>A	ENSP00000513924.1:p.Gly626Asp
ENST00000698778.1:c.1877G>A	ENSP00000513925.1:p.Gly626Asp
ENST00000698779.1:c.1877G>A	ENSP00000513926.1:p.Gly626Asp
ENST00000698801.1:n.1748G>A
ENST00000698802.1:c.1564G>A	ENSP00000513944.1:n.1564G>A
ENST00000698803.1:c.*1622G>A	ENSP00000513945.1:n.*1622G>A
ENST00000698804.1:n.4296G>A
ENST00000698805.1:n.3220G>A
ENST00000698806.1:c.*1591G>A	ENSP00000513946.1:n.*1591G>A
ENST00000698807.1:n.3939G>A
ENST00000698808.1:c.1874G>A	ENSP00000513947.1:p.Gly625Asp
ENST00000698809.1:c.1784G>A	ENSP00000513948.1:p.Gly595Asp
ENST00000698810.1:c.*1627G>A	ENSP00000513949.1:n.*1627G>A
ENST00000698812.1:c.*1883G>A	ENSP00000513950.1:n.*1883G>A
ENST00000698813.1:c.1877G>A	ENSP00000513951.1:p.Gly626Asp
ENST00000698814.1:c.1877G>A	ENSP00000513952.1:p.Gly626Asp
ENST00000698815.1:c.*54+145G>A	ENSP00000513953.1:n.*54+145G>A
ENST00000293328.8:c.1877G>A MANE Select	ENSP00000293328.3:p.Gly626Asp
ENST00000293328.7:c.1877G>A	ENSP00000293328.3:p.Gly626Asp
ENST00000468496.5:n.721G>A
ENST00000481253.2:n.292G>A
NM_012448.3:c.1877G>A , LRG_192t1:c.1877G>A	NP_036580.2:p.Gly626Asp
XM_005257625.2:c.1595G>A	XP_005257682.1:p.Gly532Asp
XM_017024977.1:c.1595G>A	XP_016880466.1:p.Gly532Asp
XM_024450897.1:c.1877G>A	XP_024306665.1:p.Gly626Asp
XM_024450898.1:c.1877G>A	XP_024306666.1:p.Gly626Asp
NM_012448.4:c.1877G>A MANE Select	NP_036580.2:p.Gly626Asp