Canonical Allele Identifier: CA404775593

Gene: IL12RB1

Linked Data

• gnomAD v4: 19-18060079-G-A
• MyVariant Identifiers: chr19:g.18170889G>A (hg19) ; chr19:g.18060079G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18060079G>A , CM000681.2:g.18060079G>A	GRCh38
NC_000019.9:g.18170889G>A , CM000681.1:g.18170889G>A	GRCh37
NC_000019.8:g.18031889G>A	NCBI36
NG_007366.2:g.43871C>T , LRG_72:g.43871C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593993.7:c.1798C>T MANE Select	ENSP00000472165.2:p.Gln600Ter
ENST00000593993.6:c.1798C>T	ENSP00000472165.2:p.Gln600Ter
ENST00000600835.6:c.1798C>T	ENSP00000470788.1:p.Gln600Ter
NM_001290023.1:c.1798C>T	NP_001276952.1:p.Gln600Ter
NM_001290024.1:c.1918C>T	NP_001276953.1:p.Gln640Ter
NM_005535.2:c.1798C>T	NP_005526.1:p.Gln600Ter
XM_006722741.2:c.1918C>T	XP_006722804.2:p.Gln640Ter
XM_011527966.1:c.1951C>T	XP_011526268.1:p.Gln651Ter
XM_011527967.1:c.1939C>T	XP_011526269.1:p.Gln647Ter
XM_011527968.1:c.1930C>T	XP_011526270.1:p.Gln644Ter
XM_011527969.1:c.1918C>T	XP_011526271.1:p.Gln640Ter
XM_011527970.1:c.1951C>T	XP_011526272.1:p.Gln651Ter
XM_011527971.1:c.1951C>T	XP_011526273.1:p.Gln651Ter
XM_011527972.1:c.1951C>T	XP_011526274.1:p.Gln651Ter
XM_011527973.1:c.1831C>T	XP_011526275.1:p.Gln611Ter
XM_011527974.1:c.1819C>T	XP_011526276.1:p.Gln607Ter
XM_011527975.1:c.1918C>T	XP_011526277.1:p.Gln640Ter
XM_006722741.3:c.1918C>T	XP_006722804.2:p.Gln640Ter
XM_011527966.2:c.1951C>T	XP_011526268.1:p.Gln651Ter
XM_011527967.2:c.1939C>T	XP_011526269.1:p.Gln647Ter
XM_011527968.3:c.1930C>T	XP_011526270.1:p.Gln644Ter
XM_011527969.2:c.1918C>T	XP_011526271.1:p.Gln640Ter
XM_011527970.2:c.1951C>T	XP_011526272.1:p.Gln651Ter
XM_011527971.3:c.1951C>T	XP_011526273.1:p.Gln651Ter
XM_011527972.3:c.1951C>T	XP_011526274.1:p.Gln651Ter
XM_011527973.2:c.1831C>T	XP_011526275.1:p.Gln611Ter
XM_011527974.2:c.1819C>T	XP_011526276.1:p.Gln607Ter
XM_011527975.2:c.1918C>T	XP_011526277.1:p.Gln640Ter
XM_017026762.1:c.1216C>T	XP_016882251.1:p.Gln406Ter
NM_001290023.2:c.1798C>T	NP_001276952.1:p.Gln600Ter
NM_005535.3:c.1798C>T MANE Select	NP_005526.1:p.Gln600Ter