Canonical Allele Identifier: CA404775523
Gene: IL12RB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18060066G>A , CM000681.2:g.18060066G>A GRCh38
NC_000019.9:g.18170876G>A , CM000681.1:g.18170876G>A GRCh37
NC_000019.8:g.18031876G>A NCBI36
NG_007366.2:g.43884C>T , LRG_72:g.43884C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000593993.7:c.1811C>T MANE Select ENSP00000472165.2:p.Pro604Leu
ENST00000593993.6:c.1811C>T ENSP00000472165.2:p.Pro604Leu
ENST00000600835.6:c.1811C>T ENSP00000470788.1:p.Pro604Leu
NM_001290023.1:c.1811C>T NP_001276952.1:p.Pro604Leu
NM_001290024.1:c.1931C>T NP_001276953.1:p.Pro644Leu
NM_005535.2:c.1811C>T NP_005526.1:p.Pro604Leu
XM_006722741.2:c.1931C>T XP_006722804.2:p.Pro644Leu
XM_011527966.1:c.1964C>T XP_011526268.1:p.Pro655Leu
XM_011527967.1:c.1952C>T XP_011526269.1:p.Pro651Leu
XM_011527968.1:c.1943C>T XP_011526270.1:p.Pro648Leu
XM_011527969.1:c.1931C>T XP_011526271.1:p.Pro644Leu
XM_011527970.1:c.1964C>T XP_011526272.1:p.Pro655Leu
XM_011527971.1:c.1964C>T XP_011526273.1:p.Pro655Leu
XM_011527972.1:c.1964C>T XP_011526274.1:p.Pro655Leu
XM_011527973.1:c.1844C>T XP_011526275.1:p.Pro615Leu
XM_011527974.1:c.1832C>T XP_011526276.1:p.Pro611Leu
XM_011527975.1:c.1931C>T XP_011526277.1:p.Pro644Leu
XM_006722741.3:c.1931C>T XP_006722804.2:p.Pro644Leu
XM_011527966.2:c.1964C>T XP_011526268.1:p.Pro655Leu
XM_011527967.2:c.1952C>T XP_011526269.1:p.Pro651Leu
XM_011527968.3:c.1943C>T XP_011526270.1:p.Pro648Leu
XM_011527969.2:c.1931C>T XP_011526271.1:p.Pro644Leu
XM_011527970.2:c.1964C>T XP_011526272.1:p.Pro655Leu
XM_011527971.3:c.1964C>T XP_011526273.1:p.Pro655Leu
XM_011527972.3:c.1964C>T XP_011526274.1:p.Pro655Leu
XM_011527973.2:c.1844C>T XP_011526275.1:p.Pro615Leu
XM_011527974.2:c.1832C>T XP_011526276.1:p.Pro611Leu
XM_011527975.2:c.1931C>T XP_011526277.1:p.Pro644Leu
XM_017026762.1:c.1229C>T XP_016882251.1:p.Pro410Leu
NM_001290023.2:c.1811C>T NP_001276952.1:p.Pro604Leu
NM_005535.3:c.1811C>T MANE Select NP_005526.1:p.Pro604Leu