Canonical Allele Identifier: CA632136045
Gene: JAK3 HGNC NCBI

Linked Data

dbSNP Id: rs1179861028
gnomAD v2: 19-17937549-G-A
gnomAD v3: 19-17826740-G-A
gnomAD v4: 19-17826740-G-A
MyVariant Identifiers: chr19:g.17937549G>A (hg19) chr19:g.17826740G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17826740G>A , CM000681.2:g.17826740G>A GRCh38
NC_000019.9:g.17937549G>A , CM000681.1:g.17937549G>A GRCh37
NC_000019.8:g.17798549G>A NCBI36
NG_007273.1:g.26252C>T , LRG_77:g.26252C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000526008.6:c.*1935C>T ENSP00000513006.1:n.*1935C>T
ENST00000696967.1:n.2555C>T
ENST00000696968.1:n.611C>T
ENST00000696969.1:n.2335C>T
ENST00000458235.7:c.*3C>T MANE Select ENSP00000391676.1:n.*3C>T
ENST00000458235.5:c.*3C>T ENSP00000391676.1:n.*3C>T
ENST00000527031.5:n.2279-1430C>T
ENST00000527670.5:c.*3C>T ENSP00000432511.1:n.*3C>T
NM_000215.3:c.*3C>T , LRG_77t1:c.*3C>T NP_000206.2:n.*3C>T
XM_005259896.2:c.*3C>T XP_005259953.1:n.*3C>T
XM_006722745.2:c.*3C>T XP_006722808.1:n.*3C>T
XM_005259896.3:c.*3C>T XP_005259953.1:n.*3C>T
NM_000215.4:c.*3C>T MANE Select NP_000206.2:n.*3C>T
Search 100 bp 5'
Search 100 bp 3'