Canonical Allele Identifier: CA506105495

Gene: JAK3

Linked Data

• dbSNP Id: rs2147682286
• MyVariant Identifiers: chr19:g.17945694G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17834885G>C , CM000681.2:g.17834885G>C	GRCh38
NC_000019.9:g.17945694G>C , CM000681.1:g.17945694G>C	GRCh37
NC_000019.8:g.17806694G>C	NCBI36
NG_007273.1:g.18107C>G , LRG_77:g.18107C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526008.6:c.*723C>G	ENSP00000513006.1:n.*723C>G
ENST00000696967.1:n.1343C>G
ENST00000696970.1:n.821C>G
ENST00000458235.7:c.2166C>G MANE Select	ENSP00000391676.1:p.Val722=
ENST00000458235.5:c.2166C>G	ENSP00000391676.1:p.Val722=
ENST00000527031.5:n.2278+1842C>G
ENST00000527670.5:c.2166C>G	ENSP00000432511.1:p.Val722=
ENST00000534444.1:c.2166C>G	ENSP00000436421.1:p.Val722=
NM_000215.3:c.2166C>G , LRG_77t1:c.2166C>G	NP_000206.2:p.Val722=
XM_005259896.2:c.2295C>G	XP_005259953.1:p.Val765=
XM_006722745.2:c.2166C>G	XP_006722808.1:p.Val722=
XM_011527990.1:c.2295C>G	XP_011526292.1:p.Val765=
XR_430137.2:n.2305C>G
XM_005259896.3:c.2295C>G	XP_005259953.1:p.Val765=
NM_000215.4:c.2166C>G MANE Select	NP_000206.2:p.Val722=