Canonical Allele Identifier: CA404774372
Gene: JAK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17843781T>G , CM000681.2:g.17843781T>G GRCh38
NC_000019.9:g.17954590T>G , CM000681.1:g.17954590T>G GRCh37
NC_000019.8:g.17815590T>G NCBI36
NG_007273.1:g.9211A>C , LRG_77:g.9211A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000526008.6:c.304A>C ENSP00000513006.1:p.Ile102Leu
ENST00000458235.7:c.304A>C MANE Select ENSP00000391676.1:p.Ile102Leu
ENST00000458235.5:c.304A>C ENSP00000391676.1:p.Ile102Leu
ENST00000526008.5:n.404A>C
ENST00000527031.5:n.394A>C
ENST00000527670.5:c.304A>C ENSP00000432511.1:p.Ile102Leu
ENST00000528293.1:n.324-290A>C
ENST00000534444.1:c.304A>C ENSP00000436421.1:p.Ile102Leu
NM_000215.3:c.304A>C , LRG_77t1:c.304A>C NP_000206.2:p.Ile102Leu
XM_005259896.2:c.433A>C XP_005259953.1:p.Ile145Leu
XM_006722745.2:c.304A>C XP_006722808.1:p.Ile102Leu
XM_011527990.1:c.433A>C XP_011526292.1:p.Ile145Leu
XM_011527991.1:c.433A>C XP_011526293.1:p.Ile145Leu
XR_430137.2:n.443A>C
XM_005259896.3:c.433A>C XP_005259953.1:p.Ile145Leu
XM_011527991.2:c.433A>C XP_011526293.1:p.Ile145Leu
NM_000215.4:c.304A>C MANE Select NP_000206.2:p.Ile102Leu