Canonical Allele Identifier: CA2326053473
Gene: JAK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17834773A= , CM000681.2:g.17834773A= GRCh38
NC_000019.9:g.17945582A= , CM000681.1:g.17945582A= GRCh37
NC_000019.8:g.17806582A= NCBI36
NG_007273.1:g.18219T= , LRG_77:g.18219T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000526008.6:c.*757-52T= ENSP00000513006.1:n.*757-52T=
ENST00000696967.1:n.1377-52T=
ENST00000696970.1:n.855-52T=
ENST00000458235.7:c.2200-52T= MANE Select ENSP00000391676.1:n.2200-52T=
ENST00000458235.5:c.2200-52T= ENSP00000391676.1:n.2200-52T=
ENST00000527031.5:n.2278+1954T=
ENST00000527670.5:c.2200-52T= ENSP00000432511.1:n.2200-52T=
ENST00000534444.1:c.2200-52T= ENSP00000436421.1:n.2200-52T=
NM_000215.3:c.2200-52T= , LRG_77t1:c.2200-52T= NP_000206.2:n.2200-52T=
XM_005259896.2:c.2329-52T= XP_005259953.1:n.2329-52T=
XM_006722745.2:c.2200-52T= XP_006722808.1:n.2200-52T=
XM_011527990.1:c.2329-52T= XP_011526292.1:n.2329-52T=
XR_430137.2:n.2339-52T=
XM_005259896.3:c.2329-52T= XP_005259953.1:n.2329-52T=
NM_000215.4:c.2200-52T= MANE Select NP_000206.2:n.2200-52T=