Canonical Allele Identifier: CA2735876268

Gene: JAK3

Linked Data

• dbSNP Id: rs2147682634

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17835051A>T , CM000681.2:g.17835051A>T	GRCh38
NC_000019.9:g.17945860A>T , CM000681.1:g.17945860A>T	GRCh37
NC_000019.8:g.17806860A>T	NCBI36
NG_007273.1:g.17941T>A , LRG_77:g.17941T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526008.6:c.*604+32T>A	ENSP00000513006.1:n.*604+32T>A
ENST00000696967.1:n.1224+32T>A
ENST00000696970.1:n.702+32T>A
ENST00000458235.7:c.2047+32T>A MANE Select	ENSP00000391676.1:n.2047+32T>A
ENST00000458235.5:c.2047+32T>A	ENSP00000391676.1:n.2047+32T>A
ENST00000527031.5:n.2278+1676T>A
ENST00000527670.5:c.2047+32T>A	ENSP00000432511.1:n.2047+32T>A
ENST00000534444.1:c.2047+32T>A	ENSP00000436421.1:n.2047+32T>A
NM_000215.3:c.2047+32T>A , LRG_77t1:c.2047+32T>A	NP_000206.2:n.2047+32T>A
XM_005259896.2:c.2176+32T>A	XP_005259953.1:n.2176+32T>A
XM_006722745.2:c.2047+32T>A	XP_006722808.1:n.2047+32T>A
XM_011527990.1:c.2176+32T>A	XP_011526292.1:n.2176+32T>A
XR_430137.2:n.2186+32T>A
XM_005259896.3:c.2176+32T>A	XP_005259953.1:n.2176+32T>A
NM_000215.4:c.2047+32T>A MANE Select	NP_000206.2:n.2047+32T>A