Canonical Allele Identifier: CA404763168
Gene: JAK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.17937683G>A (hg19) chr19:g.17826874G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17826874G>A , CM000681.2:g.17826874G>A GRCh38
NC_000019.9:g.17937683G>A , CM000681.1:g.17937683G>A GRCh37
NC_000019.8:g.17798683G>A NCBI36
NG_007273.1:g.26118C>T , LRG_77:g.26118C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000526008.6:c.*1801C>T ENSP00000513006.1:n.*1801C>T
ENST00000696967.1:n.2421C>T
ENST00000696968.1:n.477C>T
ENST00000696969.1:n.2201C>T
ENST00000458235.7:c.3244C>T MANE Select ENSP00000391676.1:p.Pro1082Ser
ENST00000458235.5:c.3244C>T ENSP00000391676.1:p.Pro1082Ser
ENST00000527031.5:n.2279-1564C>T
ENST00000527670.5:c.3244C>T ENSP00000432511.1:p.Pro1082Ser
NM_000215.3:c.3244C>T , LRG_77t1:c.3244C>T NP_000206.2:p.Pro1082Ser
XM_005259896.2:c.3373C>T XP_005259953.1:p.Pro1125Ser
XM_006722745.2:c.3244C>T XP_006722808.1:p.Pro1082Ser
XM_005259896.3:c.3373C>T XP_005259953.1:p.Pro1125Ser
NM_000215.4:c.3244C>T MANE Select NP_000206.2:p.Pro1082Ser
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