Canonical Allele Identifier: CA404778888

Gene: IL12RB1

Linked Data

• MyVariant Identifiers: chr19:g.18180461C>T (hg19) ; chr19:g.18069651C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18069651C>T , CM000681.2:g.18069651C>T	GRCh38
NC_000019.9:g.18180461C>T , CM000681.1:g.18180461C>T	GRCh37
NC_000019.8:g.18041461C>T	NCBI36
NG_007366.2:g.34299G>A , LRG_72:g.34299G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593993.7:c.1084G>A MANE Select	ENSP00000472165.2:p.Ala362Thr
ENST00000593993.6:c.1084G>A	ENSP00000472165.2:p.Ala362Thr
ENST00000600835.6:c.1084G>A	ENSP00000470788.1:p.Ala362Thr
NM_001290023.1:c.1084G>A	NP_001276952.1:p.Ala362Thr
NM_001290024.1:c.1204G>A	NP_001276953.1:p.Ala402Thr
NM_005535.2:c.1084G>A	NP_005526.1:p.Ala362Thr
XM_006722741.2:c.1204G>A	XP_006722804.2:p.Ala402Thr
XM_011527966.1:c.1237G>A	XP_011526268.1:p.Ala413Thr
XM_011527967.1:c.1225G>A	XP_011526269.1:p.Ala409Thr
XM_011527968.1:c.1216G>A	XP_011526270.1:p.Ala406Thr
XM_011527969.1:c.1204G>A	XP_011526271.1:p.Ala402Thr
XM_011527970.1:c.1237G>A	XP_011526272.1:p.Ala413Thr
XM_011527971.1:c.1237G>A	XP_011526273.1:p.Ala413Thr
XM_011527972.1:c.1237G>A	XP_011526274.1:p.Ala413Thr
XM_011527973.1:c.1117G>A	XP_011526275.1:p.Ala373Thr
XM_011527974.1:c.1105G>A	XP_011526276.1:p.Ala369Thr
XM_011527975.1:c.1204G>A	XP_011526277.1:p.Ala402Thr
XM_011527976.1:c.1237G>A	XP_011526278.1:p.Ala413Thr
XM_006722741.3:c.1204G>A	XP_006722804.2:p.Ala402Thr
XM_011527966.2:c.1237G>A	XP_011526268.1:p.Ala413Thr
XM_011527967.2:c.1225G>A	XP_011526269.1:p.Ala409Thr
XM_011527968.3:c.1216G>A	XP_011526270.1:p.Ala406Thr
XM_011527969.2:c.1204G>A	XP_011526271.1:p.Ala402Thr
XM_011527970.2:c.1237G>A	XP_011526272.1:p.Ala413Thr
XM_011527971.3:c.1237G>A	XP_011526273.1:p.Ala413Thr
XM_011527972.3:c.1237G>A	XP_011526274.1:p.Ala413Thr
XM_011527973.2:c.1117G>A	XP_011526275.1:p.Ala373Thr
XM_011527974.2:c.1105G>A	XP_011526276.1:p.Ala369Thr
XM_011527975.2:c.1204G>A	XP_011526277.1:p.Ala402Thr
XM_011527976.2:c.1237G>A	XP_011526278.1:p.Ala413Thr
XM_017026762.1:c.502G>A	XP_016882251.1:p.Ala168Thr
NM_001290023.2:c.1084G>A	NP_001276952.1:p.Ala362Thr
NM_005535.3:c.1084G>A MANE Select	NP_005526.1:p.Ala362Thr