Canonical Allele Identifier: CA290731999

Gene: STAT5B

Linked Data

• dbSNP Id: rs1052982052
• gnomAD v3: 17-42262109-A-T
• gnomAD v4: 17-42262109-A-T
• MyVariant Identifiers: chr17:g.40414127A>T (hg19) ; chr17:g.42262109A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42262109A>T , CM000679.2:g.42262109A>T	GRCh38
NC_000017.10:g.40414127A>T , CM000679.1:g.40414127A>T	GRCh37
NC_000017.9:g.37667653A>T	NCBI36
NG_007271.1:g.19298T>A , LRG_192:g.19298T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000415845.2:c.-11+14519T>A	ENSP00000398379.2:n.-11+14519T>A
ENST00000698774.1:n.164+14139T>A
ENST00000698775.1:c.-11+14139T>A	ENSP00000513922.1:n.-11+14139T>A
ENST00000698776.1:c.-11+25678T>A	ENSP00000513923.1:n.-11+25678T>A
ENST00000698777.1:c.-11+26351T>A	ENSP00000513924.1:n.-11+26351T>A
ENST00000698778.1:c.-11+14139T>A	ENSP00000513925.1:n.-11+14139T>A
ENST00000698779.1:c.-11+14139T>A	ENSP00000513926.1:n.-11+14139T>A
ENST00000698803.1:c.-11+14139T>A	ENSP00000513945.1:n.-11+14139T>A
ENST00000698804.1:n.109+14139T>A
ENST00000698805.1:n.111+14139T>A
ENST00000698806.1:c.-11+14139T>A	ENSP00000513946.1:n.-11+14139T>A
ENST00000698807.1:n.144+14139T>A
ENST00000698808.1:c.-11+14139T>A	ENSP00000513947.1:n.-11+14139T>A
ENST00000698809.1:c.-11+14139T>A	ENSP00000513948.1:n.-11+14139T>A
ENST00000698810.1:c.-11+14139T>A	ENSP00000513949.1:n.-11+14139T>A
ENST00000698813.1:c.-11+14139T>A	ENSP00000513951.1:n.-11+14139T>A
ENST00000698814.1:c.-11+14139T>A	ENSP00000513952.1:n.-11+14139T>A
ENST00000698815.1:c.-11+14139T>A	ENSP00000513953.1:n.-11+14139T>A
ENST00000698816.1:n.78+14139T>A
ENST00000293328.8:c.-11+14139T>A MANE Select	ENSP00000293328.3:n.-11+14139T>A
ENST00000293328.7:c.-11+14139T>A	ENSP00000293328.3:n.-11+14139T>A
ENST00000415845.1:c.-11+14519T>A	ENSP00000398379.1:n.-11+14519T>A
ENST00000468312.1:n.159+14139T>A
NM_012448.3:c.-11+14139T>A , LRG_192t1:c.-11+14139T>A	NP_036580.2:n.-11+14139T>A
XM_005257626.3:c.-11+14139T>A	XP_005257683.1:n.-11+14139T>A
XM_005257626.4:c.-11+14139T>A	XP_005257683.1:n.-11+14139T>A
XM_017024977.1:c.-136+14139T>A	XP_016880466.1:n.-136+14139T>A
XM_024450897.1:c.-11+25678T>A	XP_024306665.1:n.-11+25678T>A
XM_024450898.1:c.-11+6177T>A	XP_024306666.1:n.-11+6177T>A
NM_012448.4:c.-11+14139T>A MANE Select	NP_036580.2:n.-11+14139T>A