Canonical Allele Identifier: CA506002566
Gene: JAK3 HGNC NCBI

Linked Data

dbSNP Id: rs2147669697
MyVariant Identifiers: chr19:g.17937566G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17826757G>A , CM000681.2:g.17826757G>A GRCh38
NC_000019.9:g.17937566G>A , CM000681.1:g.17937566G>A GRCh37
NC_000019.8:g.17798566G>A NCBI36
NG_007273.1:g.26235C>T , LRG_77:g.26235C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000526008.6:c.*1918C>T ENSP00000513006.1:n.*1918C>T
ENST00000696967.1:n.2538C>T
ENST00000696968.1:n.594C>T
ENST00000696969.1:n.2318C>T
ENST00000458235.7:c.3361C>T MANE Select ENSP00000391676.1:p.Leu1121=
ENST00000458235.5:c.3361C>T ENSP00000391676.1:p.Leu1121=
ENST00000527031.5:n.2279-1447C>T
ENST00000527670.5:c.3361C>T ENSP00000432511.1:p.Leu1121=
NM_000215.3:c.3361C>T , LRG_77t1:c.3361C>T NP_000206.2:p.Leu1121=
XM_005259896.2:c.3490C>T XP_005259953.1:p.Leu1164=
XM_006722745.2:c.3361C>T XP_006722808.1:p.Leu1121=
XM_005259896.3:c.3490C>T XP_005259953.1:p.Leu1164=
NM_000215.4:c.3361C>T MANE Select NP_000206.2:p.Leu1121=