Canonical Allele Identifier: CA399576648

Gene: STAT5B

Linked Data

• MyVariant Identifiers: chr17:g.40362215A>G (hg19) ; chr17:g.42210197A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42210197A>G , CM000679.2:g.42210197A>G	GRCh38
NC_000017.10:g.40362215A>G , CM000679.1:g.40362215A>G	GRCh37
NC_000017.9:g.37615741A>G	NCBI36
NG_007271.1:g.71210T>C , LRG_192:g.71210T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000415845.2:c.1880T>C	ENSP00000398379.2:p.Ile627Thr
ENST00000698774.1:n.2740T>C
ENST00000698775.1:c.*1886T>C	ENSP00000513922.1:n.*1886T>C
ENST00000698776.1:c.1880T>C	ENSP00000513923.1:p.Ile627Thr
ENST00000698777.1:c.1880T>C	ENSP00000513924.1:p.Ile627Thr
ENST00000698778.1:c.1880T>C	ENSP00000513925.1:p.Ile627Thr
ENST00000698779.1:c.1880T>C	ENSP00000513926.1:p.Ile627Thr
ENST00000698801.1:n.1751T>C
ENST00000698802.1:c.1567T>C	ENSP00000513944.1:n.1567T>C
ENST00000698803.1:c.*1625T>C	ENSP00000513945.1:n.*1625T>C
ENST00000698804.1:n.4299T>C
ENST00000698805.1:n.3223T>C
ENST00000698806.1:c.*1594T>C	ENSP00000513946.1:n.*1594T>C
ENST00000698807.1:n.3942T>C
ENST00000698808.1:c.1877T>C	ENSP00000513947.1:p.Ile626Thr
ENST00000698809.1:c.1787T>C	ENSP00000513948.1:p.Ile596Thr
ENST00000698810.1:c.*1630T>C	ENSP00000513949.1:n.*1630T>C
ENST00000698812.1:c.*1886T>C	ENSP00000513950.1:n.*1886T>C
ENST00000698813.1:c.1880T>C	ENSP00000513951.1:p.Ile627Thr
ENST00000698814.1:c.1880T>C	ENSP00000513952.1:p.Ile627Thr
ENST00000698815.1:c.*54+148T>C	ENSP00000513953.1:n.*54+148T>C
ENST00000293328.8:c.1880T>C MANE Select	ENSP00000293328.3:p.Ile627Thr
ENST00000293328.7:c.1880T>C	ENSP00000293328.3:p.Ile627Thr
ENST00000468496.5:n.724T>C
ENST00000481253.2:n.295T>C
NM_012448.3:c.1880T>C , LRG_192t1:c.1880T>C	NP_036580.2:p.Ile627Thr
XM_005257625.2:c.1598T>C	XP_005257682.1:p.Ile533Thr
XM_017024977.1:c.1598T>C	XP_016880466.1:p.Ile533Thr
XM_024450897.1:c.1880T>C	XP_024306665.1:p.Ile627Thr
XM_024450898.1:c.1880T>C	XP_024306666.1:p.Ile627Thr
NM_012448.4:c.1880T>C MANE Select	NP_036580.2:p.Ile627Thr