Canonical Allele Identifier: CA2583511944

Gene: IL12RB1

Linked Data

• gnomAD v4: 19-18075643-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18075643C>A , CM000681.2:g.18075643C>A	GRCh38
NC_000019.9:g.18186453C>A , CM000681.1:g.18186453C>A	GRCh37
NC_000019.8:g.18047453C>A	NCBI36
NG_007366.2:g.28307G>T , LRG_72:g.28307G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593993.7:c.700+106G>T MANE Select	ENSP00000472165.2:n.700+106G>T
ENST00000322153.11:c.700+106G>T	ENSP00000314425.5:n.700+106G>T
ENST00000593993.6:c.700+106G>T	ENSP00000472165.2:n.700+106G>T
ENST00000600835.6:c.700+106G>T	ENSP00000470788.1:n.700+106G>T
NM_001290023.1:c.700+106G>T	NP_001276952.1:n.700+106G>T
NM_001290024.1:c.820+106G>T	NP_001276953.1:n.820+106G>T
NM_005535.2:c.700+106G>T	NP_005526.1:n.700+106G>T
NM_153701.2:c.700+106G>T	NP_714912.1:n.700+106G>T
XM_006722741.2:c.820+106G>T	XP_006722804.2:n.820+106G>T
XM_011527966.1:c.832+106G>T	XP_011526268.1:n.832+106G>T
XM_011527967.1:c.820+106G>T	XP_011526269.1:n.820+106G>T
XM_011527968.1:c.832+106G>T	XP_011526270.1:n.832+106G>T
XM_011527969.1:c.820+106G>T	XP_011526271.1:n.820+106G>T
XM_011527970.1:c.832+106G>T	XP_011526272.1:n.832+106G>T
XM_011527971.1:c.832+106G>T	XP_011526273.1:n.832+106G>T
XM_011527972.1:c.832+106G>T	XP_011526274.1:n.832+106G>T
XM_011527973.1:c.712+106G>T	XP_011526275.1:n.712+106G>T
XM_011527974.1:c.700+106G>T	XP_011526276.1:n.700+106G>T
XM_011527975.1:c.820+106G>T	XP_011526277.1:n.820+106G>T
XM_011527976.1:c.832+106G>T	XP_011526278.1:n.832+106G>T
XM_011527977.1:c.820+106G>T	XP_011526279.1:n.820+106G>T
XM_006722741.3:c.820+106G>T	XP_006722804.2:n.820+106G>T
XM_011527966.2:c.832+106G>T	XP_011526268.1:n.832+106G>T
XM_011527967.2:c.820+106G>T	XP_011526269.1:n.820+106G>T
XM_011527968.3:c.832+106G>T	XP_011526270.1:n.832+106G>T
XM_011527969.2:c.820+106G>T	XP_011526271.1:n.820+106G>T
XM_011527970.2:c.832+106G>T	XP_011526272.1:n.832+106G>T
XM_011527971.3:c.832+106G>T	XP_011526273.1:n.832+106G>T
XM_011527972.3:c.832+106G>T	XP_011526274.1:n.832+106G>T
XM_011527973.2:c.712+106G>T	XP_011526275.1:n.712+106G>T
XM_011527974.2:c.700+106G>T	XP_011526276.1:n.700+106G>T
XM_011527975.2:c.820+106G>T	XP_011526277.1:n.820+106G>T
XM_011527976.2:c.832+106G>T	XP_011526278.1:n.832+106G>T
XM_011527977.2:c.820+106G>T	XP_011526279.1:n.820+106G>T
XM_017026762.1:c.97+106G>T	XP_016882251.1:n.97+106G>T
NM_001290023.2:c.700+106G>T	NP_001276952.1:n.700+106G>T
NM_005535.3:c.700+106G>T MANE Select	NP_005526.1:n.700+106G>T
NM_153701.3:c.700+106G>T	NP_714912.1:n.700+106G>T