Canonical Allele Identifier: CA404773696
Gene: JAK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17843444C>A , CM000681.2:g.17843444C>A GRCh38
NC_000019.9:g.17954253C>A , CM000681.1:g.17954253C>A GRCh37
NC_000019.8:g.17815253C>A NCBI36
NG_007273.1:g.9548G>T , LRG_77:g.9548G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000526008.6:c.356G>T ENSP00000513006.1:p.Gly119Val
ENST00000458235.7:c.356G>T MANE Select ENSP00000391676.1:p.Gly119Val
ENST00000458235.5:c.356G>T ENSP00000391676.1:p.Gly119Val
ENST00000526008.5:n.456G>T
ENST00000527031.5:n.446G>T
ENST00000527670.5:c.356G>T ENSP00000432511.1:p.Gly119Val
ENST00000528293.1:n.371G>T
ENST00000534444.1:c.356G>T ENSP00000436421.1:p.Gly119Val
NM_000215.3:c.356G>T , LRG_77t1:c.356G>T NP_000206.2:p.Gly119Val
XM_005259896.2:c.485G>T XP_005259953.1:p.Gly162Val
XM_006722745.2:c.356G>T XP_006722808.1:p.Gly119Val
XM_011527990.1:c.485G>T XP_011526292.1:p.Gly162Val
XM_011527991.1:c.485G>T XP_011526293.1:p.Gly162Val
XR_430137.2:n.495G>T
XM_005259896.3:c.485G>T XP_005259953.1:p.Gly162Val
XM_011527991.2:c.485G>T XP_011526293.1:p.Gly162Val
NM_000215.4:c.356G>T MANE Select NP_000206.2:p.Gly119Val