Canonical Allele Identifier: CA2326054408
Gene: JAK3 HGNC NCBI

Linked Data

dbSNP Id: rs2094225556

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17836996A>G , CM000681.2:g.17836996A>G GRCh38
NC_000019.9:g.17947805A>G , CM000681.1:g.17947805A>G GRCh37
NC_000019.8:g.17808805A>G NCBI36
NG_007273.1:g.15996T>C , LRG_77:g.15996T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000526008.6:c.*343+133T>C ENSP00000513006.1:n.*343+133T>C
ENST00000696967.1:n.963+133T>C
ENST00000696970.1:n.441+133T>C
ENST00000458235.7:c.1786+133T>C MANE Select ENSP00000391676.1:n.1786+133T>C
ENST00000458235.5:c.1786+133T>C ENSP00000391676.1:n.1786+133T>C
ENST00000527031.5:n.2009T>C
ENST00000527670.5:c.1786+133T>C ENSP00000432511.1:n.1786+133T>C
ENST00000534444.1:c.1786+133T>C ENSP00000436421.1:n.1786+133T>C
NM_000215.3:c.1786+133T>C , LRG_77t1:c.1786+133T>C NP_000206.2:n.1786+133T>C
XM_005259896.2:c.1915+133T>C XP_005259953.1:n.1915+133T>C
XM_006722745.2:c.1786+133T>C XP_006722808.1:n.1786+133T>C
XM_011527990.1:c.1915+133T>C XP_011526292.1:n.1915+133T>C
XM_011527991.1:c.1916-42T>C XP_011526293.1:n.1916-42T>C
XR_430137.2:n.1925+133T>C
XM_005259896.3:c.1915+133T>C XP_005259953.1:n.1915+133T>C
XM_011527991.2:c.1916-42T>C XP_011526293.1:n.1916-42T>C
NM_000215.4:c.1786+133T>C MANE Select NP_000206.2:n.1786+133T>C