Canonical Allele Identifier: CA404763131
Gene: JAK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.17937665A>T (hg19) chr19:g.17826856A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17826856A>T , CM000681.2:g.17826856A>T GRCh38
NC_000019.9:g.17937665A>T , CM000681.1:g.17937665A>T GRCh37
NC_000019.8:g.17798665A>T NCBI36
NG_007273.1:g.26136T>A , LRG_77:g.26136T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000526008.6:c.*1819T>A ENSP00000513006.1:n.*1819T>A
ENST00000696967.1:n.2439T>A
ENST00000696968.1:n.495T>A
ENST00000696969.1:n.2219T>A
ENST00000458235.7:c.3262T>A MANE Select ENSP00000391676.1:p.Phe1088Ile
ENST00000458235.5:c.3262T>A ENSP00000391676.1:p.Phe1088Ile
ENST00000527031.5:n.2279-1546T>A
ENST00000527670.5:c.3262T>A ENSP00000432511.1:p.Phe1088Ile
NM_000215.3:c.3262T>A , LRG_77t1:c.3262T>A NP_000206.2:p.Phe1088Ile
XM_005259896.2:c.3391T>A XP_005259953.1:p.Phe1131Ile
XM_006722745.2:c.3262T>A XP_006722808.1:p.Phe1088Ile
XM_005259896.3:c.3391T>A XP_005259953.1:p.Phe1131Ile
NM_000215.4:c.3262T>A MANE Select NP_000206.2:p.Phe1088Ile
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