Canonical Allele Identifier: CA404763190
Gene: JAK3 HGNC NCBI

Linked Data

dbSNP Id: rs2147670009
gnomAD v4: 19-17826883-C-T
MyVariant Identifiers: chr19:g.17937692C>T (hg19) chr19:g.17826883C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17826883C>T , CM000681.2:g.17826883C>T GRCh38
NC_000019.9:g.17937692C>T , CM000681.1:g.17937692C>T GRCh37
NC_000019.8:g.17798692C>T NCBI36
NG_007273.1:g.26109G>A , LRG_77:g.26109G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000526008.6:c.*1792G>A ENSP00000513006.1:n.*1792G>A
ENST00000696967.1:n.2412G>A
ENST00000696968.1:n.468G>A
ENST00000696969.1:n.2192G>A
ENST00000458235.7:c.3235G>A MANE Select ENSP00000391676.1:p.Ala1079Thr
ENST00000458235.5:c.3235G>A ENSP00000391676.1:p.Ala1079Thr
ENST00000527031.5:n.2279-1573G>A
ENST00000527670.5:c.3235G>A ENSP00000432511.1:p.Ala1079Thr
NM_000215.3:c.3235G>A , LRG_77t1:c.3235G>A NP_000206.2:p.Ala1079Thr
XM_005259896.2:c.3364G>A XP_005259953.1:p.Ala1122Thr
XM_006722745.2:c.3235G>A XP_006722808.1:p.Ala1079Thr
XM_005259896.3:c.3364G>A XP_005259953.1:p.Ala1122Thr
NM_000215.4:c.3235G>A MANE Select NP_000206.2:p.Ala1079Thr
Search 100 bp 5'
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