Canonical Allele Identifier: CA404775585
Gene: IL12RB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18060078T>C , CM000681.2:g.18060078T>C GRCh38
NC_000019.9:g.18170888T>C , CM000681.1:g.18170888T>C GRCh37
NC_000019.8:g.18031888T>C NCBI36
NG_007366.2:g.43872A>G , LRG_72:g.43872A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000593993.7:c.1799A>G MANE Select ENSP00000472165.2:p.Gln600Arg
ENST00000593993.6:c.1799A>G ENSP00000472165.2:p.Gln600Arg
ENST00000600835.6:c.1799A>G ENSP00000470788.1:p.Gln600Arg
NM_001290023.1:c.1799A>G NP_001276952.1:p.Gln600Arg
NM_001290024.1:c.1919A>G NP_001276953.1:p.Gln640Arg
NM_005535.2:c.1799A>G NP_005526.1:p.Gln600Arg
XM_006722741.2:c.1919A>G XP_006722804.2:p.Gln640Arg
XM_011527966.1:c.1952A>G XP_011526268.1:p.Gln651Arg
XM_011527967.1:c.1940A>G XP_011526269.1:p.Gln647Arg
XM_011527968.1:c.1931A>G XP_011526270.1:p.Gln644Arg
XM_011527969.1:c.1919A>G XP_011526271.1:p.Gln640Arg
XM_011527970.1:c.1952A>G XP_011526272.1:p.Gln651Arg
XM_011527971.1:c.1952A>G XP_011526273.1:p.Gln651Arg
XM_011527972.1:c.1952A>G XP_011526274.1:p.Gln651Arg
XM_011527973.1:c.1832A>G XP_011526275.1:p.Gln611Arg
XM_011527974.1:c.1820A>G XP_011526276.1:p.Gln607Arg
XM_011527975.1:c.1919A>G XP_011526277.1:p.Gln640Arg
XM_006722741.3:c.1919A>G XP_006722804.2:p.Gln640Arg
XM_011527966.2:c.1952A>G XP_011526268.1:p.Gln651Arg
XM_011527967.2:c.1940A>G XP_011526269.1:p.Gln647Arg
XM_011527968.3:c.1931A>G XP_011526270.1:p.Gln644Arg
XM_011527969.2:c.1919A>G XP_011526271.1:p.Gln640Arg
XM_011527970.2:c.1952A>G XP_011526272.1:p.Gln651Arg
XM_011527971.3:c.1952A>G XP_011526273.1:p.Gln651Arg
XM_011527972.3:c.1952A>G XP_011526274.1:p.Gln651Arg
XM_011527973.2:c.1832A>G XP_011526275.1:p.Gln611Arg
XM_011527974.2:c.1820A>G XP_011526276.1:p.Gln607Arg
XM_011527975.2:c.1919A>G XP_011526277.1:p.Gln640Arg
XM_017026762.1:c.1217A>G XP_016882251.1:p.Gln406Arg
NM_001290023.2:c.1799A>G NP_001276952.1:p.Gln600Arg
NM_005535.3:c.1799A>G MANE Select NP_005526.1:p.Gln600Arg