Canonical Allele Identifier: CA404774883

Gene: IL12RB1

Linked Data

• MyVariant Identifiers: chr19:g.18170733A>T (hg19) ; chr19:g.18059923A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18059923A>T , CM000681.2:g.18059923A>T	GRCh38
NC_000019.9:g.18170733A>T , CM000681.1:g.18170733A>T	GRCh37
NC_000019.8:g.18031733A>T	NCBI36
NG_007366.2:g.44027T>A , LRG_72:g.44027T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593993.7:c.1954T>A MANE Select	ENSP00000472165.2:p.Leu652Met
ENST00000593993.6:c.1954T>A	ENSP00000472165.2:p.Leu652Met
ENST00000600835.6:c.1954T>A	ENSP00000470788.1:p.Leu652Met
NM_001290023.1:c.1954T>A	NP_001276952.1:p.Leu652Met
NM_001290024.1:c.2074T>A	NP_001276953.1:p.Leu692Met
NM_005535.2:c.1954T>A	NP_005526.1:p.Leu652Met
XM_006722741.2:c.2074T>A	XP_006722804.2:p.Leu692Met
XM_011527966.1:c.2107T>A	XP_011526268.1:p.Leu703Met
XM_011527967.1:c.2095T>A	XP_011526269.1:p.Leu699Met
XM_011527968.1:c.2086T>A	XP_011526270.1:p.Leu696Met
XM_011527969.1:c.2074T>A	XP_011526271.1:p.Leu692Met
XM_011527970.1:c.2107T>A	XP_011526272.1:p.Leu703Met
XM_011527971.1:c.2107T>A	XP_011526273.1:p.Leu703Met
XM_011527972.1:c.2107T>A	XP_011526274.1:p.Leu703Met
XM_011527973.1:c.1987T>A	XP_011526275.1:p.Leu663Met
XM_011527974.1:c.1975T>A	XP_011526276.1:p.Leu659Met
XM_011527975.1:c.2074T>A	XP_011526277.1:p.Leu692Met
XM_006722741.3:c.2074T>A	XP_006722804.2:p.Leu692Met
XM_011527966.2:c.2107T>A	XP_011526268.1:p.Leu703Met
XM_011527967.2:c.2095T>A	XP_011526269.1:p.Leu699Met
XM_011527968.3:c.2086T>A	XP_011526270.1:p.Leu696Met
XM_011527969.2:c.2074T>A	XP_011526271.1:p.Leu692Met
XM_011527970.2:c.2107T>A	XP_011526272.1:p.Leu703Met
XM_011527971.3:c.2107T>A	XP_011526273.1:p.Leu703Met
XM_011527972.3:c.2107T>A	XP_011526274.1:p.Leu703Met
XM_011527973.2:c.1987T>A	XP_011526275.1:p.Leu663Met
XM_011527974.2:c.1975T>A	XP_011526276.1:p.Leu659Met
XM_011527975.2:c.2074T>A	XP_011526277.1:p.Leu692Met
XM_017026762.1:c.1372T>A	XP_016882251.1:p.Leu458Met
NM_001290023.2:c.1954T>A	NP_001276952.1:p.Leu652Met
NM_005535.3:c.1954T>A MANE Select	NP_005526.1:p.Leu652Met