Canonical Allele Identifier: CA306119325
Gene: JAK3 HGNC NCBI

Linked Data

dbSNP Id: rs200718111
gnomAD v2: 19-17937418-A-C
gnomAD v3: 19-17826609-A-C
gnomAD v4: 19-17826609-A-C
MyVariant Identifiers: chr19:g.17937418A>C (hg19) chr19:g.17826609A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17826609A>C , CM000681.2:g.17826609A>C GRCh38
NC_000019.9:g.17937418A>C , CM000681.1:g.17937418A>C GRCh37
NC_000019.8:g.17798418A>C NCBI36
NG_007273.1:g.26383T>G , LRG_77:g.26383T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000526008.6:c.*2066T>G ENSP00000513006.1:n.*2066T>G
ENST00000696967.1:n.2686T>G
ENST00000696968.1:n.742T>G
ENST00000696969.1:n.2466T>G
ENST00000458235.7:c.*134T>G MANE Select ENSP00000391676.1:n.*134T>G
ENST00000458235.5:c.*134T>G ENSP00000391676.1:n.*134T>G
ENST00000527031.5:n.2279-1299T>G
ENST00000527670.5:c.*134T>G ENSP00000432511.1:n.*134T>G
NM_000215.3:c.*134T>G , LRG_77t1:c.*134T>G NP_000206.2:n.*134T>G
XM_005259896.2:c.*134T>G XP_005259953.1:n.*134T>G
XM_006722745.2:c.*134T>G XP_006722808.1:n.*134T>G
XM_005259896.3:c.*134T>G XP_005259953.1:n.*134T>G
NM_000215.4:c.*134T>G MANE Select NP_000206.2:n.*134T>G
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