Canonical Allele Identifier: CA772089467

Gene: STAT5B

Linked Data

• dbSNP Id: rs900993753
• gnomAD v3: 17-42262135-T-G
• gnomAD v4: 17-42262135-T-G
• MyVariant Identifiers: chr17:g.40414153T>G (hg19) ; chr17:g.42262135T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42262135T>G , CM000679.2:g.42262135T>G	GRCh38
NC_000017.10:g.40414153T>G , CM000679.1:g.40414153T>G	GRCh37
NC_000017.9:g.37667679T>G	NCBI36
NG_007271.1:g.19272A>C , LRG_192:g.19272A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000415845.2:c.-11+14493A>C	ENSP00000398379.2:n.-11+14493A>C
ENST00000698774.1:n.164+14113A>C
ENST00000698775.1:c.-11+14113A>C	ENSP00000513922.1:n.-11+14113A>C
ENST00000698776.1:c.-11+25652A>C	ENSP00000513923.1:n.-11+25652A>C
ENST00000698777.1:c.-11+26325A>C	ENSP00000513924.1:n.-11+26325A>C
ENST00000698778.1:c.-11+14113A>C	ENSP00000513925.1:n.-11+14113A>C
ENST00000698779.1:c.-11+14113A>C	ENSP00000513926.1:n.-11+14113A>C
ENST00000698803.1:c.-11+14113A>C	ENSP00000513945.1:n.-11+14113A>C
ENST00000698804.1:n.109+14113A>C
ENST00000698805.1:n.111+14113A>C
ENST00000698806.1:c.-11+14113A>C	ENSP00000513946.1:n.-11+14113A>C
ENST00000698807.1:n.144+14113A>C
ENST00000698808.1:c.-11+14113A>C	ENSP00000513947.1:n.-11+14113A>C
ENST00000698809.1:c.-11+14113A>C	ENSP00000513948.1:n.-11+14113A>C
ENST00000698810.1:c.-11+14113A>C	ENSP00000513949.1:n.-11+14113A>C
ENST00000698813.1:c.-11+14113A>C	ENSP00000513951.1:n.-11+14113A>C
ENST00000698814.1:c.-11+14113A>C	ENSP00000513952.1:n.-11+14113A>C
ENST00000698815.1:c.-11+14113A>C	ENSP00000513953.1:n.-11+14113A>C
ENST00000698816.1:n.78+14113A>C
ENST00000293328.8:c.-11+14113A>C MANE Select	ENSP00000293328.3:n.-11+14113A>C
ENST00000293328.7:c.-11+14113A>C	ENSP00000293328.3:n.-11+14113A>C
ENST00000415845.1:c.-11+14493A>C	ENSP00000398379.1:n.-11+14493A>C
ENST00000468312.1:n.159+14113A>C
NM_012448.3:c.-11+14113A>C , LRG_192t1:c.-11+14113A>C	NP_036580.2:n.-11+14113A>C
XM_005257626.3:c.-11+14113A>C	XP_005257683.1:n.-11+14113A>C
XM_005257626.4:c.-11+14113A>C	XP_005257683.1:n.-11+14113A>C
XM_017024977.1:c.-136+14113A>C	XP_016880466.1:n.-136+14113A>C
XM_024450897.1:c.-11+25652A>C	XP_024306665.1:n.-11+25652A>C
XM_024450898.1:c.-11+6151A>C	XP_024306666.1:n.-11+6151A>C
NM_012448.4:c.-11+14113A>C MANE Select	NP_036580.2:n.-11+14113A>C