Canonical Allele Identifier: CA404763950

Gene: JAK3

Linked Data

• gnomAD v4: 19-17830125-G-A
• COSMIC: COSM5706896 ; COSM5706897
• MyVariant Identifiers: chr19:g.17940934G>A (hg19) ; chr19:g.17830125G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17830125G>A , CM000681.2:g.17830125G>A	GRCh38
NC_000019.9:g.17940934G>A , CM000681.1:g.17940934G>A	GRCh37
NC_000019.8:g.17801934G>A	NCBI36
NG_007273.1:g.22867C>T , LRG_77:g.22867C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526008.6:c.*1747C>T	ENSP00000513006.1:n.*1747C>T
ENST00000696967.1:n.2367C>T
ENST00000696968.1:n.423C>T
ENST00000696969.1:n.2147C>T
ENST00000458235.7:c.3190C>T MANE Select	ENSP00000391676.1:p.Pro1064Ser
ENST00000458235.5:c.3190C>T	ENSP00000391676.1:p.Pro1064Ser
ENST00000527031.5:n.2279-4815C>T
ENST00000527670.5:c.3190C>T	ENSP00000432511.1:p.Pro1064Ser
ENST00000534444.1:c.3190C>T	ENSP00000436421.1:p.Pro1064Ser
NM_000215.3:c.3190C>T , LRG_77t1:c.3190C>T	NP_000206.2:p.Pro1064Ser
XM_005259896.2:c.3319C>T	XP_005259953.1:p.Pro1107Ser
XM_006722745.2:c.3190C>T	XP_006722808.1:p.Pro1064Ser
XM_005259896.3:c.3319C>T	XP_005259953.1:p.Pro1107Ser
NM_000215.4:c.3190C>T MANE Select	NP_000206.2:p.Pro1064Ser