Canonical Allele Identifier: CA404778931

Gene: IL12RB1

Linked Data

• MyVariant Identifiers: chr19:g.18180472C>G (hg19) ; chr19:g.18069662C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18069662C>G , CM000681.2:g.18069662C>G	GRCh38
NC_000019.9:g.18180472C>G , CM000681.1:g.18180472C>G	GRCh37
NC_000019.8:g.18041472C>G	NCBI36
NG_007366.2:g.34288G>C , LRG_72:g.34288G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593993.7:c.1073G>C MANE Select	ENSP00000472165.2:p.Trp358Ser
ENST00000593993.6:c.1073G>C	ENSP00000472165.2:p.Trp358Ser
ENST00000600835.6:c.1073G>C	ENSP00000470788.1:p.Trp358Ser
NM_001290023.1:c.1073G>C	NP_001276952.1:p.Trp358Ser
NM_001290024.1:c.1193G>C	NP_001276953.1:p.Trp398Ser
NM_005535.2:c.1073G>C	NP_005526.1:p.Trp358Ser
XM_006722741.2:c.1193G>C	XP_006722804.2:p.Trp398Ser
XM_011527966.1:c.1226G>C	XP_011526268.1:p.Trp409Ser
XM_011527967.1:c.1214G>C	XP_011526269.1:p.Trp405Ser
XM_011527968.1:c.1205G>C	XP_011526270.1:p.Trp402Ser
XM_011527969.1:c.1193G>C	XP_011526271.1:p.Trp398Ser
XM_011527970.1:c.1226G>C	XP_011526272.1:p.Trp409Ser
XM_011527971.1:c.1226G>C	XP_011526273.1:p.Trp409Ser
XM_011527972.1:c.1226G>C	XP_011526274.1:p.Trp409Ser
XM_011527973.1:c.1106G>C	XP_011526275.1:p.Trp369Ser
XM_011527974.1:c.1094G>C	XP_011526276.1:p.Trp365Ser
XM_011527975.1:c.1193G>C	XP_011526277.1:p.Trp398Ser
XM_011527976.1:c.1226G>C	XP_011526278.1:p.Trp409Ser
XM_006722741.3:c.1193G>C	XP_006722804.2:p.Trp398Ser
XM_011527966.2:c.1226G>C	XP_011526268.1:p.Trp409Ser
XM_011527967.2:c.1214G>C	XP_011526269.1:p.Trp405Ser
XM_011527968.3:c.1205G>C	XP_011526270.1:p.Trp402Ser
XM_011527969.2:c.1193G>C	XP_011526271.1:p.Trp398Ser
XM_011527970.2:c.1226G>C	XP_011526272.1:p.Trp409Ser
XM_011527971.3:c.1226G>C	XP_011526273.1:p.Trp409Ser
XM_011527972.3:c.1226G>C	XP_011526274.1:p.Trp409Ser
XM_011527973.2:c.1106G>C	XP_011526275.1:p.Trp369Ser
XM_011527974.2:c.1094G>C	XP_011526276.1:p.Trp365Ser
XM_011527975.2:c.1193G>C	XP_011526277.1:p.Trp398Ser
XM_011527976.2:c.1226G>C	XP_011526278.1:p.Trp409Ser
XM_017026762.1:c.491G>C	XP_016882251.1:p.Trp164Ser
NM_001290023.2:c.1073G>C	NP_001276952.1:p.Trp358Ser
NM_005535.3:c.1073G>C MANE Select	NP_005526.1:p.Trp358Ser