Canonical Allele Identifier: CA2326056575
Gene: JAK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17841764T= , CM000681.2:g.17841764T= GRCh38
NC_000019.9:g.17952573T= , CM000681.1:g.17952573T= GRCh37
NC_000019.8:g.17813573T= NCBI36
NG_007273.1:g.11228A= , LRG_77:g.11228A=

Transcript Alleles

HGVS Amino-acid Change
NM_000215.4:c.862-2A= MANE Select NP_000206.2:n.862-2A=
ENST00000458235.7:c.862-2A= MANE Select ENSP00000391676.1:n.862-2A=
NM_000215.3:c.862-2A= , LRG_77t1:c.862-2A= NP_000206.2:n.862-2A=
ENST00000458235.5:c.862-2A= ENSP00000391676.1:n.862-2A=
ENST00000526008.5:n.962-2A=
ENST00000526008.6:c.862-2A= ENSP00000513006.1:n.862-2A=
ENST00000527031.5:n.952-2A=
ENST00000527670.5:c.862-2A= ENSP00000432511.1:n.862-2A=
ENST00000528705.1:n.211-2A=
ENST00000534444.1:c.862-2A= ENSP00000436421.1:n.862-2A=
ENST00000696967.1:n.39-2A=
XM_005259896.2:c.991-2A= XP_005259953.1:n.991-2A=
XM_005259896.3:c.991-2A= XP_005259953.1:n.991-2A=
XM_006722745.2:c.862-2A= XP_006722808.1:n.862-2A=
XM_011527990.1:c.991-2A= XP_011526292.1:n.991-2A=
XM_011527991.1:c.991-2A= XP_011526293.1:n.991-2A=
XM_011527991.2:c.991-2A= XP_011526293.1:n.991-2A=
XR_430137.2:n.1001-2A=