Canonical Allele Identifier: CA404773790

Gene: JAK3

Linked Data

• MyVariant Identifiers: chr19:g.17954278C>G (hg19) ; chr19:g.17843469C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17843469C>G , CM000681.2:g.17843469C>G	GRCh38
NC_000019.9:g.17954278C>G , CM000681.1:g.17954278C>G	GRCh37
NC_000019.8:g.17815278C>G	NCBI36
NG_007273.1:g.9523G>C , LRG_77:g.9523G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526008.6:c.331G>C	ENSP00000513006.1:p.Gly111Arg
ENST00000458235.7:c.331G>C MANE Select	ENSP00000391676.1:p.Gly111Arg
ENST00000458235.5:c.331G>C	ENSP00000391676.1:p.Gly111Arg
ENST00000526008.5:n.431G>C
ENST00000527031.5:n.421G>C
ENST00000527670.5:c.331G>C	ENSP00000432511.1:p.Gly111Arg
ENST00000528293.1:n.346G>C
ENST00000534444.1:c.331G>C	ENSP00000436421.1:p.Gly111Arg
NM_000215.3:c.331G>C , LRG_77t1:c.331G>C	NP_000206.2:p.Gly111Arg
XM_005259896.2:c.460G>C	XP_005259953.1:p.Gly154Arg
XM_006722745.2:c.331G>C	XP_006722808.1:p.Gly111Arg
XM_011527990.1:c.460G>C	XP_011526292.1:p.Gly154Arg
XM_011527991.1:c.460G>C	XP_011526293.1:p.Gly154Arg
XR_430137.2:n.470G>C
XM_005259896.3:c.460G>C	XP_005259953.1:p.Gly154Arg
XM_011527991.2:c.460G>C	XP_011526293.1:p.Gly154Arg
NM_000215.4:c.331G>C MANE Select	NP_000206.2:p.Gly111Arg