Canonical Allele Identifier: CA404781666

Gene: IL12RB1

Linked Data

• MyVariant Identifiers: chr19:g.18186637A>C (hg19) ; chr19:g.18075827A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18075827A>C , CM000681.2:g.18075827A>C	GRCh38
NC_000019.9:g.18186637A>C , CM000681.1:g.18186637A>C	GRCh37
NC_000019.8:g.18047637A>C	NCBI36
NG_007366.2:g.28123T>G , LRG_72:g.28123T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000593993.7:c.622T>G MANE Select	ENSP00000472165.2:p.Phe208Val
ENST00000322153.11:c.622T>G	ENSP00000314425.5:p.Phe208Val
ENST00000593993.6:c.622T>G	ENSP00000472165.2:p.Phe208Val
ENST00000600835.6:c.622T>G	ENSP00000470788.1:p.Phe208Val
NM_001290023.1:c.622T>G	NP_001276952.1:p.Phe208Val
NM_001290024.1:c.742T>G	NP_001276953.1:p.Phe248Val
NM_005535.2:c.622T>G	NP_005526.1:p.Phe208Val
NM_153701.2:c.622T>G	NP_714912.1:p.Phe208Val
XM_006722741.2:c.742T>G	XP_006722804.2:p.Phe248Val
XM_011527966.1:c.754T>G	XP_011526268.1:p.Phe252Val
XM_011527967.1:c.742T>G	XP_011526269.1:p.Phe248Val
XM_011527968.1:c.754T>G	XP_011526270.1:p.Phe252Val
XM_011527969.1:c.742T>G	XP_011526271.1:p.Phe248Val
XM_011527970.1:c.754T>G	XP_011526272.1:p.Phe252Val
XM_011527971.1:c.754T>G	XP_011526273.1:p.Phe252Val
XM_011527972.1:c.754T>G	XP_011526274.1:p.Phe252Val
XM_011527973.1:c.634T>G	XP_011526275.1:p.Phe212Val
XM_011527974.1:c.622T>G	XP_011526276.1:p.Phe208Val
XM_011527975.1:c.742T>G	XP_011526277.1:p.Phe248Val
XM_011527976.1:c.754T>G	XP_011526278.1:p.Phe252Val
XM_011527977.1:c.742T>G	XP_011526279.1:p.Phe248Val
XM_006722741.3:c.742T>G	XP_006722804.2:p.Phe248Val
XM_011527966.2:c.754T>G	XP_011526268.1:p.Phe252Val
XM_011527967.2:c.742T>G	XP_011526269.1:p.Phe248Val
XM_011527968.3:c.754T>G	XP_011526270.1:p.Phe252Val
XM_011527969.2:c.742T>G	XP_011526271.1:p.Phe248Val
XM_011527970.2:c.754T>G	XP_011526272.1:p.Phe252Val
XM_011527971.3:c.754T>G	XP_011526273.1:p.Phe252Val
XM_011527972.3:c.754T>G	XP_011526274.1:p.Phe252Val
XM_011527973.2:c.634T>G	XP_011526275.1:p.Phe212Val
XM_011527974.2:c.622T>G	XP_011526276.1:p.Phe208Val
XM_011527975.2:c.742T>G	XP_011526277.1:p.Phe248Val
XM_011527976.2:c.754T>G	XP_011526278.1:p.Phe252Val
XM_011527977.2:c.742T>G	XP_011526279.1:p.Phe248Val
XM_017026762.1:c.19T>G	XP_016882251.1:p.Phe7Val
NM_001290023.2:c.622T>G	NP_001276952.1:p.Phe208Val
NM_005535.3:c.622T>G MANE Select	NP_005526.1:p.Phe208Val
NM_153701.3:c.622T>G	NP_714912.1:p.Phe208Val