Canonical Allele Identifier: CA506106052

Gene: JAK3

Linked Data

• gnomAD v4: 19-17843383-G-T
• MyVariant Identifiers: chr19:g.17954192G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17843383G>T , CM000681.2:g.17843383G>T	GRCh38
NC_000019.9:g.17954192G>T , CM000681.1:g.17954192G>T	GRCh37
NC_000019.8:g.17815192G>T	NCBI36
NG_007273.1:g.9609C>A , LRG_77:g.9609C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526008.6:c.417C>A	ENSP00000513006.1:p.Ala139=
ENST00000458235.7:c.417C>A MANE Select	ENSP00000391676.1:p.Ala139=
ENST00000458235.5:c.417C>A	ENSP00000391676.1:p.Ala139=
ENST00000526008.5:n.517C>A
ENST00000527031.5:n.507C>A
ENST00000527670.5:c.417C>A	ENSP00000432511.1:p.Ala139=
ENST00000528293.1:n.432C>A
ENST00000534444.1:c.417C>A	ENSP00000436421.1:p.Ala139=
NM_000215.3:c.417C>A , LRG_77t1:c.417C>A	NP_000206.2:p.Ala139=
XM_005259896.2:c.546C>A	XP_005259953.1:p.Ala182=
XM_006722745.2:c.417C>A	XP_006722808.1:p.Ala139=
XM_011527990.1:c.546C>A	XP_011526292.1:p.Ala182=
XM_011527991.1:c.546C>A	XP_011526293.1:p.Ala182=
XR_430137.2:n.556C>A
XM_005259896.3:c.546C>A	XP_005259953.1:p.Ala182=
XM_011527991.2:c.546C>A	XP_011526293.1:p.Ala182=
NM_000215.4:c.417C>A MANE Select	NP_000206.2:p.Ala139=