Canonical Allele Identifier: CA2326053501
Gene: JAK3 HGNC NCBI

Linked Data

dbSNP Id: rs1568402792

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17834819T>C , CM000681.2:g.17834819T>C GRCh38
NC_000019.9:g.17945628T>C , CM000681.1:g.17945628T>C GRCh37
NC_000019.8:g.17806628T>C NCBI36
NG_007273.1:g.18173A>G , LRG_77:g.18173A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000526008.6:c.*756+33A>G ENSP00000513006.1:n.*756+33A>G
ENST00000696967.1:n.1376+33A>G
ENST00000696970.1:n.854+33A>G
ENST00000458235.7:c.2199+33A>G MANE Select ENSP00000391676.1:n.2199+33A>G
ENST00000458235.5:c.2199+33A>G ENSP00000391676.1:n.2199+33A>G
ENST00000527031.5:n.2278+1908A>G
ENST00000527670.5:c.2199+33A>G ENSP00000432511.1:n.2199+33A>G
ENST00000534444.1:c.2199+33A>G ENSP00000436421.1:n.2199+33A>G
NM_000215.3:c.2199+33A>G , LRG_77t1:c.2199+33A>G NP_000206.2:n.2199+33A>G
XM_005259896.2:c.2328+33A>G XP_005259953.1:n.2328+33A>G
XM_006722745.2:c.2199+33A>G XP_006722808.1:n.2199+33A>G
XM_011527990.1:c.2328+33A>G XP_011526292.1:n.2328+33A>G
XR_430137.2:n.2338+33A>G
XM_005259896.3:c.2328+33A>G XP_005259953.1:n.2328+33A>G
NM_000215.4:c.2199+33A>G MANE Select NP_000206.2:n.2199+33A>G