Canonical Allele Identifier: CA506002579
Gene: JAK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.17937591A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17826782A>T , CM000681.2:g.17826782A>T GRCh38
NC_000019.9:g.17937591A>T , CM000681.1:g.17937591A>T GRCh37
NC_000019.8:g.17798591A>T NCBI36
NG_007273.1:g.26210T>A , LRG_77:g.26210T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000526008.6:c.*1893T>A ENSP00000513006.1:n.*1893T>A
ENST00000696967.1:n.2513T>A
ENST00000696968.1:n.569T>A
ENST00000696969.1:n.2293T>A
ENST00000458235.7:c.3336T>A MANE Select ENSP00000391676.1:p.Ala1112=
ENST00000458235.5:c.3336T>A ENSP00000391676.1:p.Ala1112=
ENST00000527031.5:n.2279-1472T>A
ENST00000527670.5:c.3336T>A ENSP00000432511.1:p.Ala1112=
NM_000215.3:c.3336T>A , LRG_77t1:c.3336T>A NP_000206.2:p.Ala1112=
XM_005259896.2:c.3465T>A XP_005259953.1:p.Ala1155=
XM_006722745.2:c.3336T>A XP_006722808.1:p.Ala1112=
XM_005259896.3:c.3465T>A XP_005259953.1:p.Ala1155=
NM_000215.4:c.3336T>A MANE Select NP_000206.2:p.Ala1112=