Canonical Allele Identifier: CA626045178

Gene: STAT5B

Linked Data

• dbSNP Id: rs1215153756
• gnomAD v2: 17-40413920-G-A
• gnomAD v3: 17-42261902-G-A
• gnomAD v4: 17-42261902-G-A
• MyVariant Identifiers: chr17:g.40413920G>A (hg19) ; chr17:g.42261902G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42261902G>A , CM000679.2:g.42261902G>A	GRCh38
NC_000017.10:g.40413920G>A , CM000679.1:g.40413920G>A	GRCh37
NC_000017.9:g.37667446G>A	NCBI36
NG_007271.1:g.19505C>T , LRG_192:g.19505C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000415845.2:c.-11+14726C>T	ENSP00000398379.2:n.-11+14726C>T
ENST00000698774.1:n.164+14346C>T
ENST00000698775.1:c.-11+14346C>T	ENSP00000513922.1:n.-11+14346C>T
ENST00000698776.1:c.-11+25885C>T	ENSP00000513923.1:n.-11+25885C>T
ENST00000698777.1:c.-11+26558C>T	ENSP00000513924.1:n.-11+26558C>T
ENST00000698778.1:c.-11+14346C>T	ENSP00000513925.1:n.-11+14346C>T
ENST00000698779.1:c.-11+14346C>T	ENSP00000513926.1:n.-11+14346C>T
ENST00000698803.1:c.-11+14346C>T	ENSP00000513945.1:n.-11+14346C>T
ENST00000698804.1:n.109+14346C>T
ENST00000698805.1:n.111+14346C>T
ENST00000698806.1:c.-11+14346C>T	ENSP00000513946.1:n.-11+14346C>T
ENST00000698807.1:n.144+14346C>T
ENST00000698808.1:c.-11+14346C>T	ENSP00000513947.1:n.-11+14346C>T
ENST00000698809.1:c.-11+14346C>T	ENSP00000513948.1:n.-11+14346C>T
ENST00000698810.1:c.-11+14346C>T	ENSP00000513949.1:n.-11+14346C>T
ENST00000698813.1:c.-11+14346C>T	ENSP00000513951.1:n.-11+14346C>T
ENST00000698814.1:c.-11+14346C>T	ENSP00000513952.1:n.-11+14346C>T
ENST00000698815.1:c.-11+14346C>T	ENSP00000513953.1:n.-11+14346C>T
ENST00000698816.1:n.78+14346C>T
ENST00000293328.8:c.-11+14346C>T MANE Select	ENSP00000293328.3:n.-11+14346C>T
ENST00000293328.7:c.-11+14346C>T	ENSP00000293328.3:n.-11+14346C>T
ENST00000415845.1:c.-11+14726C>T	ENSP00000398379.1:n.-11+14726C>T
ENST00000468312.1:n.159+14346C>T
NM_012448.3:c.-11+14346C>T , LRG_192t1:c.-11+14346C>T	NP_036580.2:n.-11+14346C>T
XM_005257626.3:c.-11+14346C>T	XP_005257683.1:n.-11+14346C>T
XM_005257626.4:c.-11+14346C>T	XP_005257683.1:n.-11+14346C>T
XM_017024977.1:c.-136+14346C>T	XP_016880466.1:n.-136+14346C>T
XM_024450897.1:c.-11+25885C>T	XP_024306665.1:n.-11+25885C>T
XM_024450898.1:c.-11+6384C>T	XP_024306666.1:n.-11+6384C>T
NM_012448.4:c.-11+14346C>T MANE Select	NP_036580.2:n.-11+14346C>T