Canonical Allele Identifier: CA306122544

Gene: JAK3

Linked Data

• dbSNP Id: rs1029796211
• gnomAD v4: 19-17830121-G-T
• MyVariant Identifiers: chr19:g.17940930G>T (hg19) ; chr19:g.17830121G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17830121G>T , CM000681.2:g.17830121G>T	GRCh38
NC_000019.9:g.17940930G>T , CM000681.1:g.17940930G>T	GRCh37
NC_000019.8:g.17801930G>T	NCBI36
NG_007273.1:g.22871C>A , LRG_77:g.22871C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526008.6:c.*1751C>A	ENSP00000513006.1:n.*1751C>A
ENST00000696967.1:n.2371C>A
ENST00000696968.1:n.427C>A
ENST00000696969.1:n.2151C>A
ENST00000458235.7:c.3194C>A MANE Select	ENSP00000391676.1:p.Ala1065Asp
ENST00000458235.5:c.3194C>A	ENSP00000391676.1:p.Ala1065Asp
ENST00000527031.5:n.2279-4811C>A
ENST00000527670.5:c.3194C>A	ENSP00000432511.1:p.Ala1065Asp
ENST00000534444.1:c.3194C>A	ENSP00000436421.1:p.Ala1065Asp
NM_000215.3:c.3194C>A , LRG_77t1:c.3194C>A	NP_000206.2:p.Ala1065Asp
XM_005259896.2:c.3323C>A	XP_005259953.1:p.Ala1108Asp
XM_006722745.2:c.3194C>A	XP_006722808.1:p.Ala1065Asp
XM_005259896.3:c.3323C>A	XP_005259953.1:p.Ala1108Asp
NM_000215.4:c.3194C>A MANE Select	NP_000206.2:p.Ala1065Asp