Canonical Allele Identifier: CA506003821

Gene: JAK3

Linked Data

• MyVariant Identifiers: chr19:g.17945417T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17834608T>G , CM000681.2:g.17834608T>G	GRCh38
NC_000019.9:g.17945417T>G , CM000681.1:g.17945417T>G	GRCh37
NC_000019.8:g.17806417T>G	NCBI36
NG_007273.1:g.18384A>C , LRG_77:g.18384A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526008.6:c.*870A>C	ENSP00000513006.1:n.*870A>C
ENST00000696967.1:n.1490A>C
ENST00000696970.1:n.968A>C
ENST00000458235.7:c.2313A>C MANE Select	ENSP00000391676.1:p.Arg771=
ENST00000458235.5:c.2313A>C	ENSP00000391676.1:p.Arg771=
ENST00000527031.5:n.2278+2119A>C
ENST00000527670.5:c.2313A>C	ENSP00000432511.1:p.Arg771=
ENST00000534444.1:c.2313A>C	ENSP00000436421.1:p.Arg771=
NM_000215.3:c.2313A>C , LRG_77t1:c.2313A>C	NP_000206.2:p.Arg771=
XM_005259896.2:c.2442A>C	XP_005259953.1:p.Arg814=
XM_006722745.2:c.2313A>C	XP_006722808.1:p.Arg771=
XM_011527990.1:c.2442A>C	XP_011526292.1:p.Arg814=
XR_430137.2:n.2452A>C
XM_005259896.3:c.2442A>C	XP_005259953.1:p.Arg814=
NM_000215.4:c.2313A>C MANE Select	NP_000206.2:p.Arg771=