Canonical Allele Identifier: CA306164081

Gene: IL12RB1

Linked Data

• dbSNP Id: rs149768779
• MyVariant Identifiers: chr19:g.18186572C>A (hg19) ; chr19:g.18075762C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18075762C>A , CM000681.2:g.18075762C>A	GRCh38
NC_000019.9:g.18186572C>A , CM000681.1:g.18186572C>A	GRCh37
NC_000019.8:g.18047572C>A	NCBI36
NG_007366.2:g.28188G>T , LRG_72:g.28188G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593993.7:c.687G>T MANE Select	ENSP00000472165.2:p.Val229=
ENST00000322153.11:c.687G>T	ENSP00000314425.5:p.Val229=
ENST00000593993.6:c.687G>T	ENSP00000472165.2:p.Val229=
ENST00000600835.6:c.687G>T	ENSP00000470788.1:p.Val229=
NM_001290023.1:c.687G>T	NP_001276952.1:p.Val229=
NM_001290024.1:c.807G>T	NP_001276953.1:p.Val269=
NM_005535.2:c.687G>T	NP_005526.1:p.Val229=
NM_153701.2:c.687G>T	NP_714912.1:p.Val229=
XM_006722741.2:c.807G>T	XP_006722804.2:p.Val269=
XM_011527966.1:c.819G>T	XP_011526268.1:p.Val273=
XM_011527967.1:c.807G>T	XP_011526269.1:p.Val269=
XM_011527968.1:c.819G>T	XP_011526270.1:p.Val273=
XM_011527969.1:c.807G>T	XP_011526271.1:p.Val269=
XM_011527970.1:c.819G>T	XP_011526272.1:p.Val273=
XM_011527971.1:c.819G>T	XP_011526273.1:p.Val273=
XM_011527972.1:c.819G>T	XP_011526274.1:p.Val273=
XM_011527973.1:c.699G>T	XP_011526275.1:p.Val233=
XM_011527974.1:c.687G>T	XP_011526276.1:p.Val229=
XM_011527975.1:c.807G>T	XP_011526277.1:p.Val269=
XM_011527976.1:c.819G>T	XP_011526278.1:p.Val273=
XM_011527977.1:c.807G>T	XP_011526279.1:p.Val269=
XM_006722741.3:c.807G>T	XP_006722804.2:p.Val269=
XM_011527966.2:c.819G>T	XP_011526268.1:p.Val273=
XM_011527967.2:c.807G>T	XP_011526269.1:p.Val269=
XM_011527968.3:c.819G>T	XP_011526270.1:p.Val273=
XM_011527969.2:c.807G>T	XP_011526271.1:p.Val269=
XM_011527970.2:c.819G>T	XP_011526272.1:p.Val273=
XM_011527971.3:c.819G>T	XP_011526273.1:p.Val273=
XM_011527972.3:c.819G>T	XP_011526274.1:p.Val273=
XM_011527973.2:c.699G>T	XP_011526275.1:p.Val233=
XM_011527974.2:c.687G>T	XP_011526276.1:p.Val229=
XM_011527975.2:c.807G>T	XP_011526277.1:p.Val269=
XM_011527976.2:c.819G>T	XP_011526278.1:p.Val273=
XM_011527977.2:c.807G>T	XP_011526279.1:p.Val269=
XM_017026762.1:c.84G>T	XP_016882251.1:p.Val28=
NM_001290023.2:c.687G>T	NP_001276952.1:p.Val229=
NM_005535.3:c.687G>T MANE Select	NP_005526.1:p.Val229=
NM_153701.3:c.687G>T	NP_714912.1:p.Val229=