Canonical Allele Identifier: CA404767377
Gene: JAK3 HGNC NCBI

Linked Data

dbSNP Id: rs778812304

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17834636T>A , CM000681.2:g.17834636T>A GRCh38
NC_000019.9:g.17945445T>A , CM000681.1:g.17945445T>A GRCh37
NC_000019.8:g.17806445T>A NCBI36
NG_007273.1:g.18356A>T , LRG_77:g.18356A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000526008.6:c.*842A>T ENSP00000513006.1:n.*842A>T
ENST00000696967.1:n.1462A>T
ENST00000696970.1:n.940A>T
ENST00000458235.7:c.2285A>T MANE Select ENSP00000391676.1:p.Tyr762Phe
ENST00000458235.5:c.2285A>T ENSP00000391676.1:p.Tyr762Phe
ENST00000527031.5:n.2278+2091A>T
ENST00000527670.5:c.2285A>T ENSP00000432511.1:p.Tyr762Phe
ENST00000534444.1:c.2285A>T ENSP00000436421.1:p.Tyr762Phe
NM_000215.3:c.2285A>T , LRG_77t1:c.2285A>T NP_000206.2:p.Tyr762Phe
XM_005259896.2:c.2414A>T XP_005259953.1:p.Tyr805Phe
XM_006722745.2:c.2285A>T XP_006722808.1:p.Tyr762Phe
XM_011527990.1:c.2414A>T XP_011526292.1:p.Tyr805Phe
XR_430137.2:n.2424A>T
XM_005259896.3:c.2414A>T XP_005259953.1:p.Tyr805Phe
NM_000215.4:c.2285A>T MANE Select NP_000206.2:p.Tyr762Phe