Canonical Allele Identifier: CA506105547

Gene: JAK3

Linked Data

• MyVariant Identifiers: chr19:g.17945718C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17834909C>G , CM000681.2:g.17834909C>G	GRCh38
NC_000019.9:g.17945718C>G , CM000681.1:g.17945718C>G	GRCh37
NC_000019.8:g.17806718C>G	NCBI36
NG_007273.1:g.18083G>C , LRG_77:g.18083G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000526008.6:c.*699G>C	ENSP00000513006.1:n.*699G>C
ENST00000696967.1:n.1319G>C
ENST00000696970.1:n.797G>C
ENST00000458235.7:c.2142G>C MANE Select	ENSP00000391676.1:p.Thr714=
ENST00000458235.5:c.2142G>C	ENSP00000391676.1:p.Thr714=
ENST00000527031.5:n.2278+1818G>C
ENST00000527670.5:c.2142G>C	ENSP00000432511.1:p.Thr714=
ENST00000534444.1:c.2142G>C	ENSP00000436421.1:p.Thr714=
NM_000215.3:c.2142G>C , LRG_77t1:c.2142G>C	NP_000206.2:p.Thr714=
XM_005259896.2:c.2271G>C	XP_005259953.1:p.Thr757=
XM_006722745.2:c.2142G>C	XP_006722808.1:p.Thr714=
XM_011527990.1:c.2271G>C	XP_011526292.1:p.Thr757=
XR_430137.2:n.2281G>C
XM_005259896.3:c.2271G>C	XP_005259953.1:p.Thr757=
NM_000215.4:c.2142G>C MANE Select	NP_000206.2:p.Thr714=