Canonical Allele Identifier: CA404767546

Gene: JAK3

Linked Data

• MyVariant Identifiers: chr19:g.17945521A>C (hg19) ; chr19:g.17834712A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17834712A>C , CM000681.2:g.17834712A>C	GRCh38
NC_000019.9:g.17945521A>C , CM000681.1:g.17945521A>C	GRCh37
NC_000019.8:g.17806521A>C	NCBI36
NG_007273.1:g.18280T>G , LRG_77:g.18280T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526008.6:c.*766T>G	ENSP00000513006.1:n.*766T>G
ENST00000696967.1:n.1386T>G
ENST00000696970.1:n.864T>G
ENST00000458235.7:c.2209T>G MANE Select	ENSP00000391676.1:p.Phe737Val
ENST00000458235.5:c.2209T>G	ENSP00000391676.1:p.Phe737Val
ENST00000527031.5:n.2278+2015T>G
ENST00000527670.5:c.2209T>G	ENSP00000432511.1:p.Phe737Val
ENST00000534444.1:c.2209T>G	ENSP00000436421.1:p.Phe737Val
NM_000215.3:c.2209T>G , LRG_77t1:c.2209T>G	NP_000206.2:p.Phe737Val
XM_005259896.2:c.2338T>G	XP_005259953.1:p.Phe780Val
XM_006722745.2:c.2209T>G	XP_006722808.1:p.Phe737Val
XM_011527990.1:c.2338T>G	XP_011526292.1:p.Phe780Val
XR_430137.2:n.2348T>G
XM_005259896.3:c.2338T>G	XP_005259953.1:p.Phe780Val
NM_000215.4:c.2209T>G MANE Select	NP_000206.2:p.Phe737Val