Canonical Allele Identifier: CA404775015

Gene: IL12RB1

Linked Data

• gnomAD v4: 19-18059953-G-T
• MyVariant Identifiers: chr19:g.18170763G>T (hg19) ; chr19:g.18059953G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18059953G>T , CM000681.2:g.18059953G>T	GRCh38
NC_000019.9:g.18170763G>T , CM000681.1:g.18170763G>T	GRCh37
NC_000019.8:g.18031763G>T	NCBI36
NG_007366.2:g.43997C>A , LRG_72:g.43997C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593993.7:c.1924C>A MANE Select	ENSP00000472165.2:p.Pro642Thr
ENST00000593993.6:c.1924C>A	ENSP00000472165.2:p.Pro642Thr
ENST00000600835.6:c.1924C>A	ENSP00000470788.1:p.Pro642Thr
NM_001290023.1:c.1924C>A	NP_001276952.1:p.Pro642Thr
NM_001290024.1:c.2044C>A	NP_001276953.1:p.Pro682Thr
NM_005535.2:c.1924C>A	NP_005526.1:p.Pro642Thr
XM_006722741.2:c.2044C>A	XP_006722804.2:p.Pro682Thr
XM_011527966.1:c.2077C>A	XP_011526268.1:p.Pro693Thr
XM_011527967.1:c.2065C>A	XP_011526269.1:p.Pro689Thr
XM_011527968.1:c.2056C>A	XP_011526270.1:p.Pro686Thr
XM_011527969.1:c.2044C>A	XP_011526271.1:p.Pro682Thr
XM_011527970.1:c.2077C>A	XP_011526272.1:p.Pro693Thr
XM_011527971.1:c.2077C>A	XP_011526273.1:p.Pro693Thr
XM_011527972.1:c.2077C>A	XP_011526274.1:p.Pro693Thr
XM_011527973.1:c.1957C>A	XP_011526275.1:p.Pro653Thr
XM_011527974.1:c.1945C>A	XP_011526276.1:p.Pro649Thr
XM_011527975.1:c.2044C>A	XP_011526277.1:p.Pro682Thr
XM_006722741.3:c.2044C>A	XP_006722804.2:p.Pro682Thr
XM_011527966.2:c.2077C>A	XP_011526268.1:p.Pro693Thr
XM_011527967.2:c.2065C>A	XP_011526269.1:p.Pro689Thr
XM_011527968.3:c.2056C>A	XP_011526270.1:p.Pro686Thr
XM_011527969.2:c.2044C>A	XP_011526271.1:p.Pro682Thr
XM_011527970.2:c.2077C>A	XP_011526272.1:p.Pro693Thr
XM_011527971.3:c.2077C>A	XP_011526273.1:p.Pro693Thr
XM_011527972.3:c.2077C>A	XP_011526274.1:p.Pro693Thr
XM_011527973.2:c.1957C>A	XP_011526275.1:p.Pro653Thr
XM_011527974.2:c.1945C>A	XP_011526276.1:p.Pro649Thr
XM_011527975.2:c.2044C>A	XP_011526277.1:p.Pro682Thr
XM_017026762.1:c.1342C>A	XP_016882251.1:p.Pro448Thr
NM_001290023.2:c.1924C>A	NP_001276952.1:p.Pro642Thr
NM_005535.3:c.1924C>A MANE Select	NP_005526.1:p.Pro642Thr