Canonical Allele Identifier: CA404764196

Gene: JAK3

Linked Data

• MyVariant Identifiers: chr19:g.17941000G>C (hg19) ; chr19:g.17830191G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17830191G>C , CM000681.2:g.17830191G>C	GRCh38
NC_000019.9:g.17941000G>C , CM000681.1:g.17941000G>C	GRCh37
NC_000019.8:g.17802000G>C	NCBI36
NG_007273.1:g.22801C>G , LRG_77:g.22801C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526008.6:c.*1681C>G	ENSP00000513006.1:n.*1681C>G
ENST00000696967.1:n.2301C>G
ENST00000696968.1:n.357C>G
ENST00000696969.1:n.2081C>G
ENST00000458235.7:c.3124C>G MANE Select	ENSP00000391676.1:p.Arg1042Gly
ENST00000458235.5:c.3124C>G	ENSP00000391676.1:p.Arg1042Gly
ENST00000527031.5:n.2279-4881C>G
ENST00000527670.5:c.3124C>G	ENSP00000432511.1:p.Arg1042Gly
ENST00000534444.1:c.3124C>G	ENSP00000436421.1:p.Arg1042Gly
NM_000215.3:c.3124C>G , LRG_77t1:c.3124C>G	NP_000206.2:p.Arg1042Gly
XM_005259896.2:c.3253C>G	XP_005259953.1:p.Arg1085Gly
XM_006722745.2:c.3124C>G	XP_006722808.1:p.Arg1042Gly
XM_005259896.3:c.3253C>G	XP_005259953.1:p.Arg1085Gly
NM_000215.4:c.3124C>G MANE Select	NP_000206.2:p.Arg1042Gly