Canonical Allele Identifier: CA404778438

Gene: IL12RB1

Linked Data

• MyVariant Identifiers: chr19:g.18180361C>G (hg19) ; chr19:g.18069551C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18069551C>G , CM000681.2:g.18069551C>G	GRCh38
NC_000019.9:g.18180361C>G , CM000681.1:g.18180361C>G	GRCh37
NC_000019.8:g.18041361C>G	NCBI36
NG_007366.2:g.34399G>C , LRG_72:g.34399G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000593993.7:c.1184G>C MANE Select	ENSP00000472165.2:p.Gly395Ala
ENST00000593993.6:c.1184G>C	ENSP00000472165.2:p.Gly395Ala
ENST00000600835.6:c.1184G>C	ENSP00000470788.1:p.Gly395Ala
NM_001290023.1:c.1184G>C	NP_001276952.1:p.Gly395Ala
NM_001290024.1:c.1304G>C	NP_001276953.1:p.Gly435Ala
NM_005535.2:c.1184G>C	NP_005526.1:p.Gly395Ala
XM_006722741.2:c.1304G>C	XP_006722804.2:p.Gly435Ala
XM_011527966.1:c.1337G>C	XP_011526268.1:p.Gly446Ala
XM_011527967.1:c.1325G>C	XP_011526269.1:p.Gly442Ala
XM_011527968.1:c.1316G>C	XP_011526270.1:p.Gly439Ala
XM_011527969.1:c.1304G>C	XP_011526271.1:p.Gly435Ala
XM_011527970.1:c.1337G>C	XP_011526272.1:p.Gly446Ala
XM_011527971.1:c.1337G>C	XP_011526273.1:p.Gly446Ala
XM_011527972.1:c.1337G>C	XP_011526274.1:p.Gly446Ala
XM_011527973.1:c.1217G>C	XP_011526275.1:p.Gly406Ala
XM_011527974.1:c.1205G>C	XP_011526276.1:p.Gly402Ala
XM_011527975.1:c.1304G>C	XP_011526277.1:p.Gly435Ala
XM_011527976.1:c.1337G>C	XP_011526278.1:p.Gly446Ala
XM_006722741.3:c.1304G>C	XP_006722804.2:p.Gly435Ala
XM_011527966.2:c.1337G>C	XP_011526268.1:p.Gly446Ala
XM_011527967.2:c.1325G>C	XP_011526269.1:p.Gly442Ala
XM_011527968.3:c.1316G>C	XP_011526270.1:p.Gly439Ala
XM_011527969.2:c.1304G>C	XP_011526271.1:p.Gly435Ala
XM_011527970.2:c.1337G>C	XP_011526272.1:p.Gly446Ala
XM_011527971.3:c.1337G>C	XP_011526273.1:p.Gly446Ala
XM_011527972.3:c.1337G>C	XP_011526274.1:p.Gly446Ala
XM_011527973.2:c.1217G>C	XP_011526275.1:p.Gly406Ala
XM_011527974.2:c.1205G>C	XP_011526276.1:p.Gly402Ala
XM_011527975.2:c.1304G>C	XP_011526277.1:p.Gly435Ala
XM_011527976.2:c.1337G>C	XP_011526278.1:p.Gly446Ala
XM_017026762.1:c.602G>C	XP_016882251.1:p.Gly201Ala
NM_001290023.2:c.1184G>C	NP_001276952.1:p.Gly395Ala
NM_005535.3:c.1184G>C MANE Select	NP_005526.1:p.Gly395Ala