Canonical Allele Identifier: CA404767312

Gene: JAK3

Linked Data

• dbSNP Id: rs2147681430
• MyVariant Identifiers: chr19:g.17945415G>A (hg19) ; chr19:g.17834606G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17834606G>A , CM000681.2:g.17834606G>A	GRCh38
NC_000019.9:g.17945415G>A , CM000681.1:g.17945415G>A	GRCh37
NC_000019.8:g.17806415G>A	NCBI36
NG_007273.1:g.18386C>T , LRG_77:g.18386C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526008.6:c.*872C>T	ENSP00000513006.1:n.*872C>T
ENST00000696967.1:n.1492C>T
ENST00000696970.1:n.970C>T
ENST00000458235.7:c.2315C>T MANE Select	ENSP00000391676.1:p.Ala772Val
ENST00000458235.5:c.2315C>T	ENSP00000391676.1:p.Ala772Val
ENST00000527031.5:n.2278+2121C>T
ENST00000527670.5:c.2315C>T	ENSP00000432511.1:p.Ala772Val
ENST00000534444.1:c.2315C>T	ENSP00000436421.1:p.Ala772Val
NM_000215.3:c.2315C>T , LRG_77t1:c.2315C>T	NP_000206.2:p.Ala772Val
XM_005259896.2:c.2444C>T	XP_005259953.1:p.Ala815Val
XM_006722745.2:c.2315C>T	XP_006722808.1:p.Ala772Val
XM_011527990.1:c.2444C>T	XP_011526292.1:p.Ala815Val
XR_430137.2:n.2454C>T
XM_005259896.3:c.2444C>T	XP_005259953.1:p.Ala815Val
NM_000215.4:c.2315C>T MANE Select	NP_000206.2:p.Ala772Val