Canonical Allele Identifier: CA404767398
Gene: JAK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17834645C>A , CM000681.2:g.17834645C>A GRCh38
NC_000019.9:g.17945454C>A , CM000681.1:g.17945454C>A GRCh37
NC_000019.8:g.17806454C>A NCBI36
NG_007273.1:g.18347G>T , LRG_77:g.18347G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000526008.6:c.*833G>T ENSP00000513006.1:n.*833G>T
ENST00000696967.1:n.1453G>T
ENST00000696970.1:n.931G>T
ENST00000458235.7:c.2276G>T MANE Select ENSP00000391676.1:p.Cys759Phe
ENST00000458235.5:c.2276G>T ENSP00000391676.1:p.Cys759Phe
ENST00000527031.5:n.2278+2082G>T
ENST00000527670.5:c.2276G>T ENSP00000432511.1:p.Cys759Phe
ENST00000534444.1:c.2276G>T ENSP00000436421.1:p.Cys759Phe
NM_000215.3:c.2276G>T , LRG_77t1:c.2276G>T NP_000206.2:p.Cys759Phe
XM_005259896.2:c.2405G>T XP_005259953.1:p.Cys802Phe
XM_006722745.2:c.2276G>T XP_006722808.1:p.Cys759Phe
XM_011527990.1:c.2405G>T XP_011526292.1:p.Cys802Phe
XR_430137.2:n.2415G>T
XM_005259896.3:c.2405G>T XP_005259953.1:p.Cys802Phe
NM_000215.4:c.2276G>T MANE Select NP_000206.2:p.Cys759Phe