Canonical Allele Identifier: CA500214977

Gene: STAT5B

Linked Data

• dbSNP Id: rs1486038634
• gnomAD v4: 17-42210199-G-T
• MyVariant Identifiers: chr17:g.40362217G>T (hg19) ; chr17:g.42210199G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42210199G>T , CM000679.2:g.42210199G>T	GRCh38
NC_000017.10:g.40362217G>T , CM000679.1:g.40362217G>T	GRCh37
NC_000017.9:g.37615743G>T	NCBI36
NG_007271.1:g.71208C>A , LRG_192:g.71208C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000415845.2:c.1878C>A	ENSP00000398379.2:p.Gly626=
ENST00000698774.1:n.2738C>A
ENST00000698775.1:c.*1884C>A	ENSP00000513922.1:n.*1884C>A
ENST00000698776.1:c.1878C>A	ENSP00000513923.1:p.Gly626=
ENST00000698777.1:c.1878C>A	ENSP00000513924.1:p.Gly626=
ENST00000698778.1:c.1878C>A	ENSP00000513925.1:p.Gly626=
ENST00000698779.1:c.1878C>A	ENSP00000513926.1:p.Gly626=
ENST00000698801.1:n.1749C>A
ENST00000698802.1:c.1565C>A	ENSP00000513944.1:n.1565C>A
ENST00000698803.1:c.*1623C>A	ENSP00000513945.1:n.*1623C>A
ENST00000698804.1:n.4297C>A
ENST00000698805.1:n.3221C>A
ENST00000698806.1:c.*1592C>A	ENSP00000513946.1:n.*1592C>A
ENST00000698807.1:n.3940C>A
ENST00000698808.1:c.1875C>A	ENSP00000513947.1:p.Gly625=
ENST00000698809.1:c.1785C>A	ENSP00000513948.1:p.Gly595=
ENST00000698810.1:c.*1628C>A	ENSP00000513949.1:n.*1628C>A
ENST00000698812.1:c.*1884C>A	ENSP00000513950.1:n.*1884C>A
ENST00000698813.1:c.1878C>A	ENSP00000513951.1:p.Gly626=
ENST00000698814.1:c.1878C>A	ENSP00000513952.1:p.Gly626=
ENST00000698815.1:c.*54+146C>A	ENSP00000513953.1:n.*54+146C>A
ENST00000293328.8:c.1878C>A MANE Select	ENSP00000293328.3:p.Gly626=
ENST00000293328.7:c.1878C>A	ENSP00000293328.3:p.Gly626=
ENST00000468496.5:n.722C>A
ENST00000481253.2:n.293C>A
NM_012448.3:c.1878C>A , LRG_192t1:c.1878C>A	NP_036580.2:p.Gly626=
XM_005257625.2:c.1596C>A	XP_005257682.1:p.Gly532=
XM_017024977.1:c.1596C>A	XP_016880466.1:p.Gly532=
XM_024450897.1:c.1878C>A	XP_024306665.1:p.Gly626=
XM_024450898.1:c.1878C>A	XP_024306666.1:p.Gly626=
NM_012448.4:c.1878C>A MANE Select	NP_036580.2:p.Gly626=