Canonical Allele Identifier: CA404778413

Gene: IL12RB1

Linked Data

• MyVariant Identifiers: chr19:g.18180355C>G (hg19) ; chr19:g.18069545C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18069545C>G , CM000681.2:g.18069545C>G	GRCh38
NC_000019.9:g.18180355C>G , CM000681.1:g.18180355C>G	GRCh37
NC_000019.8:g.18041355C>G	NCBI36
NG_007366.2:g.34405G>C , LRG_72:g.34405G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593993.7:c.1189+1G>C MANE Select	ENSP00000472165.2:n.1189+1G>C
ENST00000593993.6:c.1189+1G>C	ENSP00000472165.2:n.1189+1G>C
ENST00000600835.6:c.1189+1G>C	ENSP00000470788.1:n.1189+1G>C
NM_001290023.1:c.1189+1G>C	NP_001276952.1:n.1189+1G>C
NM_001290024.1:c.1309+1G>C	NP_001276953.1:n.1309+1G>C
NM_005535.2:c.1189+1G>C	NP_005526.1:n.1189+1G>C
XM_006722741.2:c.1309+1G>C	XP_006722804.2:n.1309+1G>C
XM_011527966.1:c.1342+1G>C	XP_011526268.1:n.1342+1G>C
XM_011527967.1:c.1330+1G>C	XP_011526269.1:n.1330+1G>C
XM_011527968.1:c.1321+1G>C	XP_011526270.1:n.1321+1G>C
XM_011527969.1:c.1309+1G>C	XP_011526271.1:n.1309+1G>C
XM_011527970.1:c.1342+1G>C	XP_011526272.1:n.1342+1G>C
XM_011527971.1:c.1342+1G>C	XP_011526273.1:n.1342+1G>C
XM_011527972.1:c.1342+1G>C	XP_011526274.1:n.1342+1G>C
XM_011527973.1:c.1222+1G>C	XP_011526275.1:n.1222+1G>C
XM_011527974.1:c.1210+1G>C	XP_011526276.1:n.1210+1G>C
XM_011527975.1:c.1309+1G>C	XP_011526277.1:n.1309+1G>C
XM_011527976.1:c.1342+1G>C	XP_011526278.1:n.1342+1G>C
XM_006722741.3:c.1309+1G>C	XP_006722804.2:n.1309+1G>C
XM_011527966.2:c.1342+1G>C	XP_011526268.1:n.1342+1G>C
XM_011527967.2:c.1330+1G>C	XP_011526269.1:n.1330+1G>C
XM_011527968.3:c.1321+1G>C	XP_011526270.1:n.1321+1G>C
XM_011527969.2:c.1309+1G>C	XP_011526271.1:n.1309+1G>C
XM_011527970.2:c.1342+1G>C	XP_011526272.1:n.1342+1G>C
XM_011527971.3:c.1342+1G>C	XP_011526273.1:n.1342+1G>C
XM_011527972.3:c.1342+1G>C	XP_011526274.1:n.1342+1G>C
XM_011527973.2:c.1222+1G>C	XP_011526275.1:n.1222+1G>C
XM_011527974.2:c.1210+1G>C	XP_011526276.1:n.1210+1G>C
XM_011527975.2:c.1309+1G>C	XP_011526277.1:n.1309+1G>C
XM_011527976.2:c.1342+1G>C	XP_011526278.1:n.1342+1G>C
XM_017026762.1:c.607+1G>C	XP_016882251.1:n.607+1G>C
NM_001290023.2:c.1189+1G>C	NP_001276952.1:n.1189+1G>C
NM_005535.3:c.1189+1G>C MANE Select	NP_005526.1:n.1189+1G>C