Canonical Allele Identifier: CA404767364
Gene: JAK3 HGNC NCBI

Linked Data

dbSNP Id: rs1460436138

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17834631G>A , CM000681.2:g.17834631G>A GRCh38
NC_000019.9:g.17945440G>A , CM000681.1:g.17945440G>A GRCh37
NC_000019.8:g.17806440G>A NCBI36
NG_007273.1:g.18361C>T , LRG_77:g.18361C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000526008.6:c.*847C>T ENSP00000513006.1:n.*847C>T
ENST00000696967.1:n.1467C>T
ENST00000696970.1:n.945C>T
ENST00000458235.7:c.2290C>T MANE Select ENSP00000391676.1:p.Pro764Ser
ENST00000458235.5:c.2290C>T ENSP00000391676.1:p.Pro764Ser
ENST00000527031.5:n.2278+2096C>T
ENST00000527670.5:c.2290C>T ENSP00000432511.1:p.Pro764Ser
ENST00000534444.1:c.2290C>T ENSP00000436421.1:p.Pro764Ser
NM_000215.3:c.2290C>T , LRG_77t1:c.2290C>T NP_000206.2:p.Pro764Ser
XM_005259896.2:c.2419C>T XP_005259953.1:p.Pro807Ser
XM_006722745.2:c.2290C>T XP_006722808.1:p.Pro764Ser
XM_011527990.1:c.2419C>T XP_011526292.1:p.Pro807Ser
XR_430137.2:n.2429C>T
XM_005259896.3:c.2419C>T XP_005259953.1:p.Pro807Ser
NM_000215.4:c.2290C>T MANE Select NP_000206.2:p.Pro764Ser