Canonical Allele Identifier: CA506002618
Gene: JAK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.17937663G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17826854G>A , CM000681.2:g.17826854G>A GRCh38
NC_000019.9:g.17937663G>A , CM000681.1:g.17937663G>A GRCh37
NC_000019.8:g.17798663G>A NCBI36
NG_007273.1:g.26138C>T , LRG_77:g.26138C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000526008.6:c.*1821C>T ENSP00000513006.1:n.*1821C>T
ENST00000696967.1:n.2441C>T
ENST00000696968.1:n.497C>T
ENST00000696969.1:n.2221C>T
ENST00000458235.7:c.3264C>T MANE Select ENSP00000391676.1:p.Phe1088=
ENST00000458235.5:c.3264C>T ENSP00000391676.1:p.Phe1088=
ENST00000527031.5:n.2279-1544C>T
ENST00000527670.5:c.3264C>T ENSP00000432511.1:p.Phe1088=
NM_000215.3:c.3264C>T , LRG_77t1:c.3264C>T NP_000206.2:p.Phe1088=
XM_005259896.2:c.3393C>T XP_005259953.1:p.Phe1131=
XM_006722745.2:c.3264C>T XP_006722808.1:p.Phe1088=
XM_005259896.3:c.3393C>T XP_005259953.1:p.Phe1131=
NM_000215.4:c.3264C>T MANE Select NP_000206.2:p.Phe1088=