Canonical Allele Identifier: CA506002936

Gene: JAK3

Linked Data

• gnomAD v4: 19-17830210-C-A
• MyVariant Identifiers: chr19:g.17941019C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17830210C>A , CM000681.2:g.17830210C>A	GRCh38
NC_000019.9:g.17941019C>A , CM000681.1:g.17941019C>A	GRCh37
NC_000019.8:g.17802019C>A	NCBI36
NG_007273.1:g.22782G>T , LRG_77:g.22782G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526008.6:c.*1662G>T	ENSP00000513006.1:n.*1662G>T
ENST00000696967.1:n.2282G>T
ENST00000696968.1:n.338G>T
ENST00000696969.1:n.2062G>T
ENST00000458235.7:c.3105G>T MANE Select	ENSP00000391676.1:p.Leu1035=
ENST00000458235.5:c.3105G>T	ENSP00000391676.1:p.Leu1035=
ENST00000527031.5:n.2279-4900G>T
ENST00000527670.5:c.3105G>T	ENSP00000432511.1:p.Leu1035=
ENST00000534444.1:c.3105G>T	ENSP00000436421.1:p.Leu1035=
NM_000215.3:c.3105G>T , LRG_77t1:c.3105G>T	NP_000206.2:p.Leu1035=
XM_005259896.2:c.3234G>T	XP_005259953.1:p.Leu1078=
XM_006722745.2:c.3105G>T	XP_006722808.1:p.Leu1035=
XM_005259896.3:c.3234G>T	XP_005259953.1:p.Leu1078=
NM_000215.4:c.3105G>T MANE Select	NP_000206.2:p.Leu1035=