Canonical Allele Identifier: CA404763196
Gene: JAK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.17937694C>G (hg19) chr19:g.17826885C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17826885C>G , CM000681.2:g.17826885C>G GRCh38
NC_000019.9:g.17937694C>G , CM000681.1:g.17937694C>G GRCh37
NC_000019.8:g.17798694C>G NCBI36
NG_007273.1:g.26107G>C , LRG_77:g.26107G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000526008.6:c.*1790G>C ENSP00000513006.1:n.*1790G>C
ENST00000696967.1:n.2410G>C
ENST00000696968.1:n.466G>C
ENST00000696969.1:n.2190G>C
ENST00000458235.7:c.3233G>C MANE Select ENSP00000391676.1:p.Trp1078Ser
ENST00000458235.5:c.3233G>C ENSP00000391676.1:p.Trp1078Ser
ENST00000527031.5:n.2279-1575G>C
ENST00000527670.5:c.3233G>C ENSP00000432511.1:p.Trp1078Ser
NM_000215.3:c.3233G>C , LRG_77t1:c.3233G>C NP_000206.2:p.Trp1078Ser
XM_005259896.2:c.3362G>C XP_005259953.1:p.Trp1121Ser
XM_006722745.2:c.3233G>C XP_006722808.1:p.Trp1078Ser
XM_005259896.3:c.3362G>C XP_005259953.1:p.Trp1121Ser
NM_000215.4:c.3233G>C MANE Select NP_000206.2:p.Trp1078Ser
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