Canonical Allele Identifier: CA404773196
Gene: JAK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17843097C>G , CM000681.2:g.17843097C>G GRCh38
NC_000019.9:g.17953906C>G , CM000681.1:g.17953906C>G GRCh37
NC_000019.8:g.17814906C>G NCBI36
NG_007273.1:g.9895G>C , LRG_77:g.9895G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000526008.6:c.496G>C ENSP00000513006.1:p.Ala166Pro
ENST00000458235.7:c.496G>C MANE Select ENSP00000391676.1:p.Ala166Pro
ENST00000458235.5:c.496G>C ENSP00000391676.1:p.Ala166Pro
ENST00000526008.5:n.596G>C
ENST00000527031.5:n.586G>C
ENST00000527670.5:c.496G>C ENSP00000432511.1:p.Ala166Pro
ENST00000528293.1:n.511G>C
ENST00000534444.1:c.496G>C ENSP00000436421.1:p.Ala166Pro
NM_000215.3:c.496G>C , LRG_77t1:c.496G>C NP_000206.2:p.Ala166Pro
XM_005259896.2:c.625G>C XP_005259953.1:p.Ala209Pro
XM_006722745.2:c.496G>C XP_006722808.1:p.Ala166Pro
XM_011527990.1:c.625G>C XP_011526292.1:p.Ala209Pro
XM_011527991.1:c.625G>C XP_011526293.1:p.Ala209Pro
XR_430137.2:n.635G>C
XM_005259896.3:c.625G>C XP_005259953.1:p.Ala209Pro
XM_011527991.2:c.625G>C XP_011526293.1:p.Ala209Pro
NM_000215.4:c.496G>C MANE Select NP_000206.2:p.Ala166Pro