Canonical Allele Identifier: CA506032297
Gene: IL12RB1 HGNC NCBI

Linked Data

dbSNP Id: rs2146310633
MyVariant Identifiers: chr19:g.18186587C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18075777C>T , CM000681.2:g.18075777C>T GRCh38
NC_000019.9:g.18186587C>T , CM000681.1:g.18186587C>T GRCh37
NC_000019.8:g.18047587C>T NCBI36
NG_007366.2:g.28173G>A , LRG_72:g.28173G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000593993.7:c.672G>A MANE Select ENSP00000472165.2:p.Lys224=
ENST00000322153.11:c.672G>A ENSP00000314425.5:p.Lys224=
ENST00000593993.6:c.672G>A ENSP00000472165.2:p.Lys224=
ENST00000600835.6:c.672G>A ENSP00000470788.1:p.Lys224=
NM_001290023.1:c.672G>A NP_001276952.1:p.Lys224=
NM_001290024.1:c.792G>A NP_001276953.1:p.Lys264=
NM_005535.2:c.672G>A NP_005526.1:p.Lys224=
NM_153701.2:c.672G>A NP_714912.1:p.Lys224=
XM_006722741.2:c.792G>A XP_006722804.2:p.Lys264=
XM_011527966.1:c.804G>A XP_011526268.1:p.Lys268=
XM_011527967.1:c.792G>A XP_011526269.1:p.Lys264=
XM_011527968.1:c.804G>A XP_011526270.1:p.Lys268=
XM_011527969.1:c.792G>A XP_011526271.1:p.Lys264=
XM_011527970.1:c.804G>A XP_011526272.1:p.Lys268=
XM_011527971.1:c.804G>A XP_011526273.1:p.Lys268=
XM_011527972.1:c.804G>A XP_011526274.1:p.Lys268=
XM_011527973.1:c.684G>A XP_011526275.1:p.Lys228=
XM_011527974.1:c.672G>A XP_011526276.1:p.Lys224=
XM_011527975.1:c.792G>A XP_011526277.1:p.Lys264=
XM_011527976.1:c.804G>A XP_011526278.1:p.Lys268=
XM_011527977.1:c.792G>A XP_011526279.1:p.Lys264=
XM_006722741.3:c.792G>A XP_006722804.2:p.Lys264=
XM_011527966.2:c.804G>A XP_011526268.1:p.Lys268=
XM_011527967.2:c.792G>A XP_011526269.1:p.Lys264=
XM_011527968.3:c.804G>A XP_011526270.1:p.Lys268=
XM_011527969.2:c.792G>A XP_011526271.1:p.Lys264=
XM_011527970.2:c.804G>A XP_011526272.1:p.Lys268=
XM_011527971.3:c.804G>A XP_011526273.1:p.Lys268=
XM_011527972.3:c.804G>A XP_011526274.1:p.Lys268=
XM_011527973.2:c.684G>A XP_011526275.1:p.Lys228=
XM_011527974.2:c.672G>A XP_011526276.1:p.Lys224=
XM_011527975.2:c.792G>A XP_011526277.1:p.Lys264=
XM_011527976.2:c.804G>A XP_011526278.1:p.Lys268=
XM_011527977.2:c.792G>A XP_011526279.1:p.Lys264=
XM_017026762.1:c.69G>A XP_016882251.1:p.Lys23=
NM_001290023.2:c.672G>A NP_001276952.1:p.Lys224=
NM_005535.3:c.672G>A MANE Select NP_005526.1:p.Lys224=
NM_153701.3:c.672G>A NP_714912.1:p.Lys224=