Canonical Allele Identifier: CA2260394028

Gene: STAT5B

Linked Data

• dbSNP Id: rs6503691

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42242072C>A , CM000679.2:g.42242072C>A	GRCh38
NC_000017.10:g.40394090C>A , CM000679.1:g.40394090C>A	GRCh37
NC_000017.9:g.37647616C>A	NCBI36
NG_007271.1:g.39335G>T , LRG_192:g.39335G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000415845.2:c.-10-9935G>T	ENSP00000398379.2:n.-10-9935G>T
ENST00000698774.1:n.165-9935G>T
ENST00000698775.1:c.-10-9935G>T	ENSP00000513922.1:n.-10-9935G>T
ENST00000698776.1:c.-10-9935G>T	ENSP00000513923.1:n.-10-9935G>T
ENST00000698777.1:c.-10-9935G>T	ENSP00000513924.1:n.-10-9935G>T
ENST00000698778.1:c.-10-9935G>T	ENSP00000513925.1:n.-10-9935G>T
ENST00000698779.1:c.-10-9935G>T	ENSP00000513926.1:n.-10-9935G>T
ENST00000698803.1:c.-10-9935G>T	ENSP00000513945.1:n.-10-9935G>T
ENST00000698804.1:n.110-9935G>T
ENST00000698805.1:n.112-9935G>T
ENST00000698806.1:c.-10-9935G>T	ENSP00000513946.1:n.-10-9935G>T
ENST00000698807.1:n.145-9935G>T
ENST00000698808.1:c.-10-9935G>T	ENSP00000513947.1:n.-10-9935G>T
ENST00000698809.1:c.-10-9935G>T	ENSP00000513948.1:n.-10-9935G>T
ENST00000698810.1:c.-10-9935G>T	ENSP00000513949.1:n.-10-9935G>T
ENST00000698813.1:c.-10-9935G>T	ENSP00000513951.1:n.-10-9935G>T
ENST00000698814.1:c.-10-9935G>T	ENSP00000513952.1:n.-10-9935G>T
ENST00000698815.1:c.-10-9935G>T	ENSP00000513953.1:n.-10-9935G>T
ENST00000698816.1:n.79-9935G>T
ENST00000293328.8:c.-10-9935G>T MANE Select	ENSP00000293328.3:n.-10-9935G>T
ENST00000293328.7:c.-10-9935G>T	ENSP00000293328.3:n.-10-9935G>T
ENST00000415845.1:c.-10-9935G>T	ENSP00000398379.1:n.-10-9935G>T
ENST00000468312.1:n.160-9935G>T
NM_012448.3:c.-10-9935G>T , LRG_192t1:c.-10-9935G>T	NP_036580.2:n.-10-9935G>T
XM_005257626.3:c.-10-9935G>T	XP_005257683.1:n.-10-9935G>T
XM_005257626.4:c.-10-9935G>T	XP_005257683.1:n.-10-9935G>T
XM_017024977.1:c.-135-9935G>T	XP_016880466.1:n.-135-9935G>T
XM_024450897.1:c.-10-9935G>T	XP_024306665.1:n.-10-9935G>T
XM_024450898.1:c.-10-9935G>T	XP_024306666.1:n.-10-9935G>T
NM_012448.4:c.-10-9935G>T MANE Select	NP_036580.2:n.-10-9935G>T