Canonical Allele Identifier: CA783871686
Gene: JAK3 HGNC NCBI

Linked Data

dbSNP Id: rs1413142536
gnomAD v4: 19-17826669-G-A
MyVariant Identifiers: chr19:g.17937478G>A (hg19) chr19:g.17826669G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17826669G>A , CM000681.2:g.17826669G>A GRCh38
NC_000019.9:g.17937478G>A , CM000681.1:g.17937478G>A GRCh37
NC_000019.8:g.17798478G>A NCBI36
NG_007273.1:g.26323C>T , LRG_77:g.26323C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000526008.6:c.*2006C>T ENSP00000513006.1:n.*2006C>T
ENST00000696967.1:n.2626C>T
ENST00000696968.1:n.682C>T
ENST00000696969.1:n.2406C>T
ENST00000458235.7:c.*74C>T MANE Select ENSP00000391676.1:n.*74C>T
ENST00000458235.5:c.*74C>T ENSP00000391676.1:n.*74C>T
ENST00000527031.5:n.2279-1359C>T
ENST00000527670.5:c.*74C>T ENSP00000432511.1:n.*74C>T
NM_000215.3:c.*74C>T , LRG_77t1:c.*74C>T NP_000206.2:n.*74C>T
XM_005259896.2:c.*74C>T XP_005259953.1:n.*74C>T
XM_006722745.2:c.*74C>T XP_006722808.1:n.*74C>T
XM_005259896.3:c.*74C>T XP_005259953.1:n.*74C>T
NM_000215.4:c.*74C>T MANE Select NP_000206.2:n.*74C>T
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