Canonical Allele Identifier: CA404775418
Gene: IL12RB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18060043A>G , CM000681.2:g.18060043A>G GRCh38
NC_000019.9:g.18170853A>G , CM000681.1:g.18170853A>G GRCh37
NC_000019.8:g.18031853A>G NCBI36
NG_007366.2:g.43907T>C , LRG_72:g.43907T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000593993.7:c.1834T>C MANE Select ENSP00000472165.2:p.Ser612Pro
ENST00000593993.6:c.1834T>C ENSP00000472165.2:p.Ser612Pro
ENST00000600835.6:c.1834T>C ENSP00000470788.1:p.Ser612Pro
NM_001290023.1:c.1834T>C NP_001276952.1:p.Ser612Pro
NM_001290024.1:c.1954T>C NP_001276953.1:p.Ser652Pro
NM_005535.2:c.1834T>C NP_005526.1:p.Ser612Pro
XM_006722741.2:c.1954T>C XP_006722804.2:p.Ser652Pro
XM_011527966.1:c.1987T>C XP_011526268.1:p.Ser663Pro
XM_011527967.1:c.1975T>C XP_011526269.1:p.Ser659Pro
XM_011527968.1:c.1966T>C XP_011526270.1:p.Ser656Pro
XM_011527969.1:c.1954T>C XP_011526271.1:p.Ser652Pro
XM_011527970.1:c.1987T>C XP_011526272.1:p.Ser663Pro
XM_011527971.1:c.1987T>C XP_011526273.1:p.Ser663Pro
XM_011527972.1:c.1987T>C XP_011526274.1:p.Ser663Pro
XM_011527973.1:c.1867T>C XP_011526275.1:p.Ser623Pro
XM_011527974.1:c.1855T>C XP_011526276.1:p.Ser619Pro
XM_011527975.1:c.1954T>C XP_011526277.1:p.Ser652Pro
XM_006722741.3:c.1954T>C XP_006722804.2:p.Ser652Pro
XM_011527966.2:c.1987T>C XP_011526268.1:p.Ser663Pro
XM_011527967.2:c.1975T>C XP_011526269.1:p.Ser659Pro
XM_011527968.3:c.1966T>C XP_011526270.1:p.Ser656Pro
XM_011527969.2:c.1954T>C XP_011526271.1:p.Ser652Pro
XM_011527970.2:c.1987T>C XP_011526272.1:p.Ser663Pro
XM_011527971.3:c.1987T>C XP_011526273.1:p.Ser663Pro
XM_011527972.3:c.1987T>C XP_011526274.1:p.Ser663Pro
XM_011527973.2:c.1867T>C XP_011526275.1:p.Ser623Pro
XM_011527974.2:c.1855T>C XP_011526276.1:p.Ser619Pro
XM_011527975.2:c.1954T>C XP_011526277.1:p.Ser652Pro
XM_017026762.1:c.1252T>C XP_016882251.1:p.Ser418Pro
NM_001290023.2:c.1834T>C NP_001276952.1:p.Ser612Pro
NM_005535.3:c.1834T>C MANE Select NP_005526.1:p.Ser612Pro