Canonical Allele Identifier: CA404768100
Gene: JAK3 HGNC NCBI

Linked Data

dbSNP Id: rs747076404

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17835088A>T , CM000681.2:g.17835088A>T GRCh38
NC_000019.9:g.17945897A>T , CM000681.1:g.17945897A>T GRCh37
NC_000019.8:g.17806897A>T NCBI36
NG_007273.1:g.17904T>A , LRG_77:g.17904T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000526008.6:c.*599T>A ENSP00000513006.1:n.*599T>A
ENST00000696967.1:n.1219T>A
ENST00000696970.1:n.697T>A
ENST00000458235.7:c.2042T>A MANE Select ENSP00000391676.1:p.Leu681Gln
ENST00000458235.5:c.2042T>A ENSP00000391676.1:p.Leu681Gln
ENST00000527031.5:n.2278+1639T>A
ENST00000527670.5:c.2042T>A ENSP00000432511.1:p.Leu681Gln
ENST00000534444.1:c.2042T>A ENSP00000436421.1:p.Leu681Gln
NM_000215.3:c.2042T>A , LRG_77t1:c.2042T>A NP_000206.2:p.Leu681Gln
XM_005259896.2:c.2171T>A XP_005259953.1:p.Leu724Gln
XM_006722745.2:c.2042T>A XP_006722808.1:p.Leu681Gln
XM_011527990.1:c.2171T>A XP_011526292.1:p.Leu724Gln
XR_430137.2:n.2181T>A
XM_005259896.3:c.2171T>A XP_005259953.1:p.Leu724Gln
NM_000215.4:c.2042T>A MANE Select NP_000206.2:p.Leu681Gln