Canonical Allele Identifier: CA2260379900
Gene: STAT5B HGNC NCBI

Linked Data

dbSNP Id: rs2080116494

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42210096C>A , CM000679.2:g.42210096C>A GRCh38
NC_000017.10:g.40362114C>A , CM000679.1:g.40362114C>A GRCh37
NC_000017.9:g.37615640C>A NCBI36
NG_007271.1:g.71311G>T , LRG_192:g.71311G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000415845.2:c.1906+75G>T ENSP00000398379.2:n.1906+75G>T
ENST00000698774.1:n.2766+75G>T
ENST00000698775.1:c.*1912+75G>T ENSP00000513922.1:n.*1912+75G>T
ENST00000698776.1:c.1906+75G>T ENSP00000513923.1:n.1906+75G>T
ENST00000698777.1:c.1906+75G>T ENSP00000513924.1:n.1906+75G>T
ENST00000698778.1:c.1906+75G>T ENSP00000513925.1:n.1906+75G>T
ENST00000698779.1:c.1906+75G>T ENSP00000513926.1:n.1906+75G>T
ENST00000698801.1:n.1777+75G>T
ENST00000698802.1:c.1593+75G>T ENSP00000513944.1:n.1593+75G>T
ENST00000698803.1:c.*1651+75G>T ENSP00000513945.1:n.*1651+75G>T
ENST00000698804.1:n.4325+75G>T
ENST00000698805.1:n.3249+75G>T
ENST00000698806.1:c.*1620+75G>T ENSP00000513946.1:n.*1620+75G>T
ENST00000698807.1:n.3968+75G>T
ENST00000698808.1:c.1903+75G>T ENSP00000513947.1:n.1903+75G>T
ENST00000698809.1:c.1813+75G>T ENSP00000513948.1:n.1813+75G>T
ENST00000698810.1:c.*1656+75G>T ENSP00000513949.1:n.*1656+75G>T
ENST00000698812.1:c.*1912+75G>T ENSP00000513950.1:n.*1912+75G>T
ENST00000698813.1:c.1906+75G>T ENSP00000513951.1:n.1906+75G>T
ENST00000698814.1:c.1906+75G>T ENSP00000513952.1:n.1906+75G>T
ENST00000698815.1:c.*54+249G>T ENSP00000513953.1:n.*54+249G>T
ENST00000293328.8:c.1906+75G>T MANE Select ENSP00000293328.3:n.1906+75G>T
ENST00000293328.7:c.1906+75G>T ENSP00000293328.3:n.1906+75G>T
ENST00000468496.5:n.750+75G>T
ENST00000481253.2:n.321+75G>T
NM_012448.3:c.1906+75G>T , LRG_192t1:c.1906+75G>T NP_036580.2:n.1906+75G>T
XM_005257625.2:c.1624+75G>T XP_005257682.1:n.1624+75G>T
XM_017024977.1:c.1624+75G>T XP_016880466.1:n.1624+75G>T
XM_024450897.1:c.1906+75G>T XP_024306665.1:n.1906+75G>T
XM_024450898.1:c.1906+75G>T XP_024306666.1:n.1906+75G>T
NM_012448.4:c.1906+75G>T MANE Select NP_036580.2:n.1906+75G>T