Canonical Allele Identifier: CA404767682

Gene: JAK3

Linked Data

• MyVariant Identifiers: chr19:g.17945707A>G (hg19) ; chr19:g.17834898A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17834898A>G , CM000681.2:g.17834898A>G	GRCh38
NC_000019.9:g.17945707A>G , CM000681.1:g.17945707A>G	GRCh37
NC_000019.8:g.17806707A>G	NCBI36
NG_007273.1:g.18094T>C , LRG_77:g.18094T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526008.6:c.*710T>C	ENSP00000513006.1:n.*710T>C
ENST00000696967.1:n.1330T>C
ENST00000696970.1:n.808T>C
ENST00000458235.7:c.2153T>C MANE Select	ENSP00000391676.1:p.Val718Ala
ENST00000458235.5:c.2153T>C	ENSP00000391676.1:p.Val718Ala
ENST00000527031.5:n.2278+1829T>C
ENST00000527670.5:c.2153T>C	ENSP00000432511.1:p.Val718Ala
ENST00000534444.1:c.2153T>C	ENSP00000436421.1:p.Val718Ala
NM_000215.3:c.2153T>C , LRG_77t1:c.2153T>C	NP_000206.2:p.Val718Ala
XM_005259896.2:c.2282T>C	XP_005259953.1:p.Val761Ala
XM_006722745.2:c.2153T>C	XP_006722808.1:p.Val718Ala
XM_011527990.1:c.2282T>C	XP_011526292.1:p.Val761Ala
XR_430137.2:n.2292T>C
XM_005259896.3:c.2282T>C	XP_005259953.1:p.Val761Ala
NM_000215.4:c.2153T>C MANE Select	NP_000206.2:p.Val718Ala