Canonical Allele Identifier: CA404775533

Gene: IL12RB1

Linked Data

• dbSNP Id: rs1477984922
• gnomAD v4: 19-18060067-G-T
• MyVariant Identifiers: chr19:g.18170877G>T (hg19) ; chr19:g.18060067G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18060067G>T , CM000681.2:g.18060067G>T	GRCh38
NC_000019.9:g.18170877G>T , CM000681.1:g.18170877G>T	GRCh37
NC_000019.8:g.18031877G>T	NCBI36
NG_007366.2:g.43883C>A , LRG_72:g.43883C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593993.7:c.1810C>A MANE Select	ENSP00000472165.2:p.Pro604Thr
ENST00000593993.6:c.1810C>A	ENSP00000472165.2:p.Pro604Thr
ENST00000600835.6:c.1810C>A	ENSP00000470788.1:p.Pro604Thr
NM_001290023.1:c.1810C>A	NP_001276952.1:p.Pro604Thr
NM_001290024.1:c.1930C>A	NP_001276953.1:p.Pro644Thr
NM_005535.2:c.1810C>A	NP_005526.1:p.Pro604Thr
XM_006722741.2:c.1930C>A	XP_006722804.2:p.Pro644Thr
XM_011527966.1:c.1963C>A	XP_011526268.1:p.Pro655Thr
XM_011527967.1:c.1951C>A	XP_011526269.1:p.Pro651Thr
XM_011527968.1:c.1942C>A	XP_011526270.1:p.Pro648Thr
XM_011527969.1:c.1930C>A	XP_011526271.1:p.Pro644Thr
XM_011527970.1:c.1963C>A	XP_011526272.1:p.Pro655Thr
XM_011527971.1:c.1963C>A	XP_011526273.1:p.Pro655Thr
XM_011527972.1:c.1963C>A	XP_011526274.1:p.Pro655Thr
XM_011527973.1:c.1843C>A	XP_011526275.1:p.Pro615Thr
XM_011527974.1:c.1831C>A	XP_011526276.1:p.Pro611Thr
XM_011527975.1:c.1930C>A	XP_011526277.1:p.Pro644Thr
XM_006722741.3:c.1930C>A	XP_006722804.2:p.Pro644Thr
XM_011527966.2:c.1963C>A	XP_011526268.1:p.Pro655Thr
XM_011527967.2:c.1951C>A	XP_011526269.1:p.Pro651Thr
XM_011527968.3:c.1942C>A	XP_011526270.1:p.Pro648Thr
XM_011527969.2:c.1930C>A	XP_011526271.1:p.Pro644Thr
XM_011527970.2:c.1963C>A	XP_011526272.1:p.Pro655Thr
XM_011527971.3:c.1963C>A	XP_011526273.1:p.Pro655Thr
XM_011527972.3:c.1963C>A	XP_011526274.1:p.Pro655Thr
XM_011527973.2:c.1843C>A	XP_011526275.1:p.Pro615Thr
XM_011527974.2:c.1831C>A	XP_011526276.1:p.Pro611Thr
XM_011527975.2:c.1930C>A	XP_011526277.1:p.Pro644Thr
XM_017026762.1:c.1228C>A	XP_016882251.1:p.Pro410Thr
NM_001290023.2:c.1810C>A	NP_001276952.1:p.Pro604Thr
NM_005535.3:c.1810C>A MANE Select	NP_005526.1:p.Pro604Thr