Canonical Allele Identifier: CA500214971

Gene: STAT5B

Linked Data

• MyVariant Identifiers: chr17:g.40362214G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42210196G>T , CM000679.2:g.42210196G>T	GRCh38
NC_000017.10:g.40362214G>T , CM000679.1:g.40362214G>T	GRCh37
NC_000017.9:g.37615740G>T	NCBI36
NG_007271.1:g.71211C>A , LRG_192:g.71211C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000415845.2:c.1881C>A	ENSP00000398379.2:p.Ile627=
ENST00000698774.1:n.2741C>A
ENST00000698775.1:c.*1887C>A	ENSP00000513922.1:n.*1887C>A
ENST00000698776.1:c.1881C>A	ENSP00000513923.1:p.Ile627=
ENST00000698777.1:c.1881C>A	ENSP00000513924.1:p.Ile627=
ENST00000698778.1:c.1881C>A	ENSP00000513925.1:p.Ile627=
ENST00000698779.1:c.1881C>A	ENSP00000513926.1:p.Ile627=
ENST00000698801.1:n.1752C>A
ENST00000698802.1:c.1568C>A	ENSP00000513944.1:n.1568C>A
ENST00000698803.1:c.*1626C>A	ENSP00000513945.1:n.*1626C>A
ENST00000698804.1:n.4300C>A
ENST00000698805.1:n.3224C>A
ENST00000698806.1:c.*1595C>A	ENSP00000513946.1:n.*1595C>A
ENST00000698807.1:n.3943C>A
ENST00000698808.1:c.1878C>A	ENSP00000513947.1:p.Ile626=
ENST00000698809.1:c.1788C>A	ENSP00000513948.1:p.Ile596=
ENST00000698810.1:c.*1631C>A	ENSP00000513949.1:n.*1631C>A
ENST00000698812.1:c.*1887C>A	ENSP00000513950.1:n.*1887C>A
ENST00000698813.1:c.1881C>A	ENSP00000513951.1:p.Ile627=
ENST00000698814.1:c.1881C>A	ENSP00000513952.1:p.Ile627=
ENST00000698815.1:c.*54+149C>A	ENSP00000513953.1:n.*54+149C>A
ENST00000293328.8:c.1881C>A MANE Select	ENSP00000293328.3:p.Ile627=
ENST00000293328.7:c.1881C>A	ENSP00000293328.3:p.Ile627=
ENST00000468496.5:n.725C>A
ENST00000481253.2:n.296C>A
NM_012448.3:c.1881C>A , LRG_192t1:c.1881C>A	NP_036580.2:p.Ile627=
XM_005257625.2:c.1599C>A	XP_005257682.1:p.Ile533=
XM_017024977.1:c.1599C>A	XP_016880466.1:p.Ile533=
XM_024450897.1:c.1881C>A	XP_024306665.1:p.Ile627=
XM_024450898.1:c.1881C>A	XP_024306666.1:p.Ile627=
NM_012448.4:c.1881C>A MANE Select	NP_036580.2:p.Ile627=