Canonical Allele Identifier: CA404775202
Gene: IL12RB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18059997T>A , CM000681.2:g.18059997T>A GRCh38
NC_000019.9:g.18170807T>A , CM000681.1:g.18170807T>A GRCh37
NC_000019.8:g.18031807T>A NCBI36
NG_007366.2:g.43953A>T , LRG_72:g.43953A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000593993.7:c.1880A>T MANE Select ENSP00000472165.2:p.Glu627Val
ENST00000593993.6:c.1880A>T ENSP00000472165.2:p.Glu627Val
ENST00000600835.6:c.1880A>T ENSP00000470788.1:p.Glu627Val
NM_001290023.1:c.1880A>T NP_001276952.1:p.Glu627Val
NM_001290024.1:c.2000A>T NP_001276953.1:p.Glu667Val
NM_005535.2:c.1880A>T NP_005526.1:p.Glu627Val
XM_006722741.2:c.2000A>T XP_006722804.2:p.Glu667Val
XM_011527966.1:c.2033A>T XP_011526268.1:p.Glu678Val
XM_011527967.1:c.2021A>T XP_011526269.1:p.Glu674Val
XM_011527968.1:c.2012A>T XP_011526270.1:p.Glu671Val
XM_011527969.1:c.2000A>T XP_011526271.1:p.Glu667Val
XM_011527970.1:c.2033A>T XP_011526272.1:p.Glu678Val
XM_011527971.1:c.2033A>T XP_011526273.1:p.Glu678Val
XM_011527972.1:c.2033A>T XP_011526274.1:p.Glu678Val
XM_011527973.1:c.1913A>T XP_011526275.1:p.Glu638Val
XM_011527974.1:c.1901A>T XP_011526276.1:p.Glu634Val
XM_011527975.1:c.2000A>T XP_011526277.1:p.Glu667Val
XM_006722741.3:c.2000A>T XP_006722804.2:p.Glu667Val
XM_011527966.2:c.2033A>T XP_011526268.1:p.Glu678Val
XM_011527967.2:c.2021A>T XP_011526269.1:p.Glu674Val
XM_011527968.3:c.2012A>T XP_011526270.1:p.Glu671Val
XM_011527969.2:c.2000A>T XP_011526271.1:p.Glu667Val
XM_011527970.2:c.2033A>T XP_011526272.1:p.Glu678Val
XM_011527971.3:c.2033A>T XP_011526273.1:p.Glu678Val
XM_011527972.3:c.2033A>T XP_011526274.1:p.Glu678Val
XM_011527973.2:c.1913A>T XP_011526275.1:p.Glu638Val
XM_011527974.2:c.1901A>T XP_011526276.1:p.Glu634Val
XM_011527975.2:c.2000A>T XP_011526277.1:p.Glu667Val
XM_017026762.1:c.1298A>T XP_016882251.1:p.Glu433Val
NM_001290023.2:c.1880A>T NP_001276952.1:p.Glu627Val
NM_005535.3:c.1880A>T MANE Select NP_005526.1:p.Glu627Val