Canonical Allele Identifier: CA404767872

Gene: JAK3

Linked Data

• MyVariant Identifiers: chr19:g.17945759T>G (hg19) ; chr19:g.17834950T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17834950T>G , CM000681.2:g.17834950T>G	GRCh38
NC_000019.9:g.17945759T>G , CM000681.1:g.17945759T>G	GRCh37
NC_000019.8:g.17806759T>G	NCBI36
NG_007273.1:g.18042A>C , LRG_77:g.18042A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526008.6:c.*658A>C	ENSP00000513006.1:n.*658A>C
ENST00000696967.1:n.1278A>C
ENST00000696970.1:n.756A>C
ENST00000458235.7:c.2101A>C MANE Select	ENSP00000391676.1:p.Thr701Pro
ENST00000458235.5:c.2101A>C	ENSP00000391676.1:p.Thr701Pro
ENST00000527031.5:n.2278+1777A>C
ENST00000527670.5:c.2101A>C	ENSP00000432511.1:p.Thr701Pro
ENST00000534444.1:c.2101A>C	ENSP00000436421.1:p.Thr701Pro
NM_000215.3:c.2101A>C , LRG_77t1:c.2101A>C	NP_000206.2:p.Thr701Pro
XM_005259896.2:c.2230A>C	XP_005259953.1:p.Thr744Pro
XM_006722745.2:c.2101A>C	XP_006722808.1:p.Thr701Pro
XM_011527990.1:c.2230A>C	XP_011526292.1:p.Thr744Pro
XR_430137.2:n.2240A>C
XM_005259896.3:c.2230A>C	XP_005259953.1:p.Thr744Pro
NM_000215.4:c.2101A>C MANE Select	NP_000206.2:p.Thr701Pro