Canonical Allele Identifier: CA290731970
Gene: STAT5B HGNC NCBI

Linked Data

dbSNP Id: rs11079041

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42262061T>A , CM000679.2:g.42262061T>A GRCh38
NC_000017.10:g.40414079T>A , CM000679.1:g.40414079T>A GRCh37
NC_000017.9:g.37667605T>A NCBI36
NG_007271.1:g.19346A>T , LRG_192:g.19346A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000415845.2:c.-11+14567A>T ENSP00000398379.2:n.-11+14567A>T
ENST00000698774.1:n.164+14187A>T
ENST00000698775.1:c.-11+14187A>T ENSP00000513922.1:n.-11+14187A>T
ENST00000698776.1:c.-11+25726A>T ENSP00000513923.1:n.-11+25726A>T
ENST00000698777.1:c.-11+26399A>T ENSP00000513924.1:n.-11+26399A>T
ENST00000698778.1:c.-11+14187A>T ENSP00000513925.1:n.-11+14187A>T
ENST00000698779.1:c.-11+14187A>T ENSP00000513926.1:n.-11+14187A>T
ENST00000698803.1:c.-11+14187A>T ENSP00000513945.1:n.-11+14187A>T
ENST00000698804.1:n.109+14187A>T
ENST00000698805.1:n.111+14187A>T
ENST00000698806.1:c.-11+14187A>T ENSP00000513946.1:n.-11+14187A>T
ENST00000698807.1:n.144+14187A>T
ENST00000698808.1:c.-11+14187A>T ENSP00000513947.1:n.-11+14187A>T
ENST00000698809.1:c.-11+14187A>T ENSP00000513948.1:n.-11+14187A>T
ENST00000698810.1:c.-11+14187A>T ENSP00000513949.1:n.-11+14187A>T
ENST00000698813.1:c.-11+14187A>T ENSP00000513951.1:n.-11+14187A>T
ENST00000698814.1:c.-11+14187A>T ENSP00000513952.1:n.-11+14187A>T
ENST00000698815.1:c.-11+14187A>T ENSP00000513953.1:n.-11+14187A>T
ENST00000698816.1:n.78+14187A>T
ENST00000293328.8:c.-11+14187A>T MANE Select ENSP00000293328.3:n.-11+14187A>T
ENST00000293328.7:c.-11+14187A>T ENSP00000293328.3:n.-11+14187A>T
ENST00000415845.1:c.-11+14567A>T ENSP00000398379.1:n.-11+14567A>T
ENST00000468312.1:n.159+14187A>T
NM_012448.3:c.-11+14187A>T , LRG_192t1:c.-11+14187A>T NP_036580.2:n.-11+14187A>T
XM_005257626.3:c.-11+14187A>T XP_005257683.1:n.-11+14187A>T
XM_005257626.4:c.-11+14187A>T XP_005257683.1:n.-11+14187A>T
XM_017024977.1:c.-136+14187A>T XP_016880466.1:n.-136+14187A>T
XM_024450897.1:c.-11+25726A>T XP_024306665.1:n.-11+25726A>T
XM_024450898.1:c.-11+6225A>T XP_024306666.1:n.-11+6225A>T
NM_012448.4:c.-11+14187A>T MANE Select NP_036580.2:n.-11+14187A>T