Canonical Allele Identifier: CA2813814874
Gene: JAK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17829941C>G , CM000681.2:g.17829941C>G GRCh38
NC_000019.9:g.17940750C>G , CM000681.1:g.17940750C>G GRCh37
NC_000019.8:g.17801750C>G NCBI36
NG_007273.1:g.23051G>C , LRG_77:g.23051G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000526008.6:c.*1764+167G>C ENSP00000513006.1:n.*1764+167G>C
ENST00000696967.1:n.2384+167G>C
ENST00000696968.1:n.440+167G>C
ENST00000696969.1:n.2164+167G>C
ENST00000458235.7:c.3207+167G>C MANE Select ENSP00000391676.1:n.3207+167G>C
ENST00000458235.5:c.3207+167G>C ENSP00000391676.1:n.3207+167G>C
ENST00000527031.5:n.2279-4631G>C
ENST00000527670.5:c.3207+167G>C ENSP00000432511.1:n.3207+167G>C
ENST00000534444.1:c.*89G>C ENSP00000436421.1:n.*89G>C
NM_000215.3:c.3207+167G>C , LRG_77t1:c.3207+167G>C NP_000206.2:n.3207+167G>C
XM_005259896.2:c.3336+167G>C XP_005259953.1:n.3336+167G>C
XM_006722745.2:c.3207+167G>C XP_006722808.1:n.3207+167G>C
XM_005259896.3:c.3336+167G>C XP_005259953.1:n.3336+167G>C
NM_000215.4:c.3207+167G>C MANE Select NP_000206.2:n.3207+167G>C