Canonical Allele Identifier: CA404768114

Gene: JAK3

Linked Data

• MyVariant Identifiers: chr19:g.17945901T>C (hg19) ; chr19:g.17835092T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17835092T>C , CM000681.2:g.17835092T>C	GRCh38
NC_000019.9:g.17945901T>C , CM000681.1:g.17945901T>C	GRCh37
NC_000019.8:g.17806901T>C	NCBI36
NG_007273.1:g.17900A>G , LRG_77:g.17900A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526008.6:c.*595A>G	ENSP00000513006.1:n.*595A>G
ENST00000696967.1:n.1215A>G
ENST00000696970.1:n.693A>G
ENST00000458235.7:c.2038A>G MANE Select	ENSP00000391676.1:p.Ser680Gly
ENST00000458235.5:c.2038A>G	ENSP00000391676.1:p.Ser680Gly
ENST00000527031.5:n.2278+1635A>G
ENST00000527670.5:c.2038A>G	ENSP00000432511.1:p.Ser680Gly
ENST00000534444.1:c.2038A>G	ENSP00000436421.1:p.Ser680Gly
NM_000215.3:c.2038A>G , LRG_77t1:c.2038A>G	NP_000206.2:p.Ser680Gly
XM_005259896.2:c.2167A>G	XP_005259953.1:p.Ser723Gly
XM_006722745.2:c.2038A>G	XP_006722808.1:p.Ser680Gly
XM_011527990.1:c.2167A>G	XP_011526292.1:p.Ser723Gly
XR_430137.2:n.2177A>G
XM_005259896.3:c.2167A>G	XP_005259953.1:p.Ser723Gly
NM_000215.4:c.2038A>G MANE Select	NP_000206.2:p.Ser680Gly