Canonical Allele Identifier: CA2326051185
Gene: JAK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17829958G= , CM000681.2:g.17829958G= GRCh38
NC_000019.9:g.17940767G= , CM000681.1:g.17940767G= GRCh37
NC_000019.8:g.17801767G= NCBI36
NG_007273.1:g.23034C= , LRG_77:g.23034C=

Transcript Alleles

HGVS Amino-acid change
ENST00000526008.6:c.*1764+150C= ENSP00000513006.1:n.*1764+150C=
ENST00000696967.1:n.2384+150C=
ENST00000696968.1:n.440+150C=
ENST00000696969.1:n.2164+150C=
ENST00000458235.7:c.3207+150C= MANE Select ENSP00000391676.1:n.3207+150C=
ENST00000458235.5:c.3207+150C= ENSP00000391676.1:n.3207+150C=
ENST00000527031.5:n.2279-4648C=
ENST00000527670.5:c.3207+150C= ENSP00000432511.1:n.3207+150C=
ENST00000534444.1:c.*72C= ENSP00000436421.1:n.*72C=
NM_000215.3:c.3207+150C= , LRG_77t1:c.3207+150C= NP_000206.2:n.3207+150C=
XM_005259896.2:c.3336+150C= XP_005259953.1:n.3336+150C=
XM_006722745.2:c.3207+150C= XP_006722808.1:n.3207+150C=
XM_005259896.3:c.3336+150C= XP_005259953.1:n.3336+150C=
NM_000215.4:c.3207+150C= MANE Select NP_000206.2:n.3207+150C=