Canonical Allele Identifier: CA404773356

Gene: JAK3

Linked Data

• dbSNP Id: rs2147698979
• gnomAD v4: 19-17843142-G-A
• MyVariant Identifiers: chr19:g.17953951G>A (hg19) ; chr19:g.17843142G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17843142G>A , CM000681.2:g.17843142G>A	GRCh38
NC_000019.9:g.17953951G>A , CM000681.1:g.17953951G>A	GRCh37
NC_000019.8:g.17814951G>A	NCBI36
NG_007273.1:g.9850C>T , LRG_77:g.9850C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000526008.6:c.451C>T	ENSP00000513006.1:p.Pro151Ser
ENST00000458235.7:c.451C>T MANE Select	ENSP00000391676.1:p.Pro151Ser
ENST00000458235.5:c.451C>T	ENSP00000391676.1:p.Pro151Ser
ENST00000526008.5:n.551C>T
ENST00000527031.5:n.541C>T
ENST00000527670.5:c.451C>T	ENSP00000432511.1:p.Pro151Ser
ENST00000528293.1:n.466C>T
ENST00000534444.1:c.451C>T	ENSP00000436421.1:p.Pro151Ser
NM_000215.3:c.451C>T , LRG_77t1:c.451C>T	NP_000206.2:p.Pro151Ser
XM_005259896.2:c.580C>T	XP_005259953.1:p.Pro194Ser
XM_006722745.2:c.451C>T	XP_006722808.1:p.Pro151Ser
XM_011527990.1:c.580C>T	XP_011526292.1:p.Pro194Ser
XM_011527991.1:c.580C>T	XP_011526293.1:p.Pro194Ser
XR_430137.2:n.590C>T
XM_005259896.3:c.580C>T	XP_005259953.1:p.Pro194Ser
XM_011527991.2:c.580C>T	XP_011526293.1:p.Pro194Ser
NM_000215.4:c.451C>T MANE Select	NP_000206.2:p.Pro151Ser