Canonical Allele Identifier: CA290731933

Gene: STAT5B

Linked Data

• dbSNP Id: rs559566370
• gnomAD v3: 17-42261997-G-A
• gnomAD v4: 17-42261997-G-A
• MyVariant Identifiers: chr17:g.40414015G>A (hg19) ; chr17:g.42261997G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42261997G>A , CM000679.2:g.42261997G>A	GRCh38
NC_000017.10:g.40414015G>A , CM000679.1:g.40414015G>A	GRCh37
NC_000017.9:g.37667541G>A	NCBI36
NG_007271.1:g.19410C>T , LRG_192:g.19410C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000415845.2:c.-11+14631C>T	ENSP00000398379.2:n.-11+14631C>T
ENST00000698774.1:n.164+14251C>T
ENST00000698775.1:c.-11+14251C>T	ENSP00000513922.1:n.-11+14251C>T
ENST00000698776.1:c.-11+25790C>T	ENSP00000513923.1:n.-11+25790C>T
ENST00000698777.1:c.-11+26463C>T	ENSP00000513924.1:n.-11+26463C>T
ENST00000698778.1:c.-11+14251C>T	ENSP00000513925.1:n.-11+14251C>T
ENST00000698779.1:c.-11+14251C>T	ENSP00000513926.1:n.-11+14251C>T
ENST00000698803.1:c.-11+14251C>T	ENSP00000513945.1:n.-11+14251C>T
ENST00000698804.1:n.109+14251C>T
ENST00000698805.1:n.111+14251C>T
ENST00000698806.1:c.-11+14251C>T	ENSP00000513946.1:n.-11+14251C>T
ENST00000698807.1:n.144+14251C>T
ENST00000698808.1:c.-11+14251C>T	ENSP00000513947.1:n.-11+14251C>T
ENST00000698809.1:c.-11+14251C>T	ENSP00000513948.1:n.-11+14251C>T
ENST00000698810.1:c.-11+14251C>T	ENSP00000513949.1:n.-11+14251C>T
ENST00000698813.1:c.-11+14251C>T	ENSP00000513951.1:n.-11+14251C>T
ENST00000698814.1:c.-11+14251C>T	ENSP00000513952.1:n.-11+14251C>T
ENST00000698815.1:c.-11+14251C>T	ENSP00000513953.1:n.-11+14251C>T
ENST00000698816.1:n.78+14251C>T
ENST00000293328.8:c.-11+14251C>T MANE Select	ENSP00000293328.3:n.-11+14251C>T
ENST00000293328.7:c.-11+14251C>T	ENSP00000293328.3:n.-11+14251C>T
ENST00000415845.1:c.-11+14631C>T	ENSP00000398379.1:n.-11+14631C>T
ENST00000468312.1:n.159+14251C>T
NM_012448.3:c.-11+14251C>T , LRG_192t1:c.-11+14251C>T	NP_036580.2:n.-11+14251C>T
XM_005257626.3:c.-11+14251C>T	XP_005257683.1:n.-11+14251C>T
XM_005257626.4:c.-11+14251C>T	XP_005257683.1:n.-11+14251C>T
XM_017024977.1:c.-136+14251C>T	XP_016880466.1:n.-136+14251C>T
XM_024450897.1:c.-11+25790C>T	XP_024306665.1:n.-11+25790C>T
XM_024450898.1:c.-11+6289C>T	XP_024306666.1:n.-11+6289C>T
NM_012448.4:c.-11+14251C>T MANE Select	NP_036580.2:n.-11+14251C>T