Canonical Allele Identifier: CA404763082
Gene: JAK3 HGNC NCBI

Linked Data

dbSNP Id: rs2147669898
MyVariant Identifiers: chr19:g.17937640T>A (hg19) chr19:g.17826831T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17826831T>A , CM000681.2:g.17826831T>A GRCh38
NC_000019.9:g.17937640T>A , CM000681.1:g.17937640T>A GRCh37
NC_000019.8:g.17798640T>A NCBI36
NG_007273.1:g.26161A>T , LRG_77:g.26161A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000526008.6:c.*1844A>T ENSP00000513006.1:n.*1844A>T
ENST00000696967.1:n.2464A>T
ENST00000696968.1:n.520A>T
ENST00000696969.1:n.2244A>T
ENST00000458235.7:c.3287A>T MANE Select ENSP00000391676.1:p.Asp1096Val
ENST00000458235.5:c.3287A>T ENSP00000391676.1:p.Asp1096Val
ENST00000527031.5:n.2279-1521A>T
ENST00000527670.5:c.3287A>T ENSP00000432511.1:p.Asp1096Val
NM_000215.3:c.3287A>T , LRG_77t1:c.3287A>T NP_000206.2:p.Asp1096Val
XM_005259896.2:c.3416A>T XP_005259953.1:p.Asp1139Val
XM_006722745.2:c.3287A>T XP_006722808.1:p.Asp1096Val
XM_005259896.3:c.3416A>T XP_005259953.1:p.Asp1139Val
NM_000215.4:c.3287A>T MANE Select NP_000206.2:p.Asp1096Val
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