Canonical Allele Identifier: CA2583421868
Gene: JAK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17829946T>G , CM000681.2:g.17829946T>G GRCh38
NC_000019.9:g.17940755T>G , CM000681.1:g.17940755T>G GRCh37
NC_000019.8:g.17801755T>G NCBI36
NG_007273.1:g.23046A>C , LRG_77:g.23046A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000526008.6:c.*1764+162A>C ENSP00000513006.1:n.*1764+162A>C
ENST00000696967.1:n.2384+162A>C
ENST00000696968.1:n.440+162A>C
ENST00000696969.1:n.2164+162A>C
ENST00000458235.7:c.3207+162A>C MANE Select ENSP00000391676.1:n.3207+162A>C
ENST00000458235.5:c.3207+162A>C ENSP00000391676.1:n.3207+162A>C
ENST00000527031.5:n.2279-4636A>C
ENST00000527670.5:c.3207+162A>C ENSP00000432511.1:n.3207+162A>C
ENST00000534444.1:c.*84A>C ENSP00000436421.1:n.*84A>C
NM_000215.3:c.3207+162A>C , LRG_77t1:c.3207+162A>C NP_000206.2:n.3207+162A>C
XM_005259896.2:c.3336+162A>C XP_005259953.1:n.3336+162A>C
XM_006722745.2:c.3207+162A>C XP_006722808.1:n.3207+162A>C
XM_005259896.3:c.3336+162A>C XP_005259953.1:n.3336+162A>C
NM_000215.4:c.3207+162A>C MANE Select NP_000206.2:n.3207+162A>C