Canonical Allele Identifier: CA117691
Gene: STAT5B HGNC NCBI

Linked Data

ClinVar Variation Id: 5697
ClinVar RCV Id: RCV000006051
dbSNP Id: rs121908502

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42223478G>A , CM000679.2:g.42223478G>A GRCh38
NC_000017.10:g.40375496G>A , CM000679.1:g.40375496G>A GRCh37
NC_000017.9:g.37629022G>A NCBI36
NG_007271.1:g.57929C>T , LRG_192:g.57929C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000415845.2:c.454C>T ENSP00000398379.2:p.Arg152Ter
ENST00000698774.1:n.628C>T
ENST00000698775.1:c.*460C>T ENSP00000513922.1:n.*460C>T
ENST00000698776.1:c.454C>T ENSP00000513923.1:p.Arg152Ter
ENST00000698777.1:c.454C>T ENSP00000513924.1:p.Arg152Ter
ENST00000698778.1:c.454C>T ENSP00000513925.1:p.Arg152Ter
ENST00000698779.1:c.454C>T ENSP00000513926.1:p.Arg152Ter
ENST00000698801.1:n.330C>T
ENST00000698802.1:c.297C>T ENSP00000513944.1:n.297C>T
ENST00000698803.1:c.*204C>T ENSP00000513945.1:n.*204C>T
ENST00000698804.1:n.1795C>T
ENST00000698805.1:n.1797C>T
ENST00000698806.1:c.*168C>T ENSP00000513946.1:n.*168C>T
ENST00000698807.1:n.1830C>T
ENST00000698808.1:c.454C>T ENSP00000513947.1:p.Arg152Ter
ENST00000698809.1:c.454C>T ENSP00000513948.1:p.Arg152Ter
ENST00000698810.1:c.*204C>T ENSP00000513949.1:n.*204C>T
ENST00000698812.1:c.*460C>T ENSP00000513950.1:n.*460C>T
ENST00000698813.1:c.454C>T ENSP00000513951.1:p.Arg152Ter
ENST00000698814.1:c.454C>T ENSP00000513952.1:p.Arg152Ter
ENST00000698815.1:c.454C>T ENSP00000513953.1:p.Arg152Ter
ENST00000698816.1:n.542C>T
ENST00000698817.1:n.1688C>T
ENST00000293328.8:c.454C>T MANE Select ENSP00000293328.3:p.Arg152Ter
ENST00000293328.7:c.454C>T ENSP00000293328.3:p.Arg152Ter
ENST00000415845.1:c.454C>T ENSP00000398379.1:p.Arg152Ter
ENST00000468312.1:n.623C>T
NM_012448.3:c.454C>T , LRG_192t1:c.454C>T NP_036580.2:p.Arg152Ter
XM_005257625.2:c.172C>T XP_005257682.1:p.Arg58Ter
XM_005257626.3:c.454C>T XP_005257683.1:p.Arg152Ter
XM_005257626.4:c.454C>T XP_005257683.1:p.Arg152Ter
XM_017024977.1:c.172C>T XP_016880466.1:p.Arg58Ter
XM_024450897.1:c.454C>T XP_024306665.1:p.Arg152Ter
XM_024450898.1:c.454C>T XP_024306666.1:p.Arg152Ter
NM_012448.4:c.454C>T MANE Select NP_036580.2:p.Arg152Ter