Canonical Allele Identifier: CA306158744

Gene: IL12RB1

Linked Data

• dbSNP Id: rs1003563647
• MyVariant Identifiers: chr19:g.18170747T>C (hg19) ; chr19:g.18059937T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18059937T>C , CM000681.2:g.18059937T>C	GRCh38
NC_000019.9:g.18170747T>C , CM000681.1:g.18170747T>C	GRCh37
NC_000019.8:g.18031747T>C	NCBI36
NG_007366.2:g.44013A>G , LRG_72:g.44013A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593993.7:c.1940A>G MANE Select	ENSP00000472165.2:p.Asp647Gly
ENST00000593993.6:c.1940A>G	ENSP00000472165.2:p.Asp647Gly
ENST00000600835.6:c.1940A>G	ENSP00000470788.1:p.Asp647Gly
NM_001290023.1:c.1940A>G	NP_001276952.1:p.Asp647Gly
NM_001290024.1:c.2060A>G	NP_001276953.1:p.Asp687Gly
NM_005535.2:c.1940A>G	NP_005526.1:p.Asp647Gly
XM_006722741.2:c.2060A>G	XP_006722804.2:p.Asp687Gly
XM_011527966.1:c.2093A>G	XP_011526268.1:p.Asp698Gly
XM_011527967.1:c.2081A>G	XP_011526269.1:p.Asp694Gly
XM_011527968.1:c.2072A>G	XP_011526270.1:p.Asp691Gly
XM_011527969.1:c.2060A>G	XP_011526271.1:p.Asp687Gly
XM_011527970.1:c.2093A>G	XP_011526272.1:p.Asp698Gly
XM_011527971.1:c.2093A>G	XP_011526273.1:p.Asp698Gly
XM_011527972.1:c.2093A>G	XP_011526274.1:p.Asp698Gly
XM_011527973.1:c.1973A>G	XP_011526275.1:p.Asp658Gly
XM_011527974.1:c.1961A>G	XP_011526276.1:p.Asp654Gly
XM_011527975.1:c.2060A>G	XP_011526277.1:p.Asp687Gly
XM_006722741.3:c.2060A>G	XP_006722804.2:p.Asp687Gly
XM_011527966.2:c.2093A>G	XP_011526268.1:p.Asp698Gly
XM_011527967.2:c.2081A>G	XP_011526269.1:p.Asp694Gly
XM_011527968.3:c.2072A>G	XP_011526270.1:p.Asp691Gly
XM_011527969.2:c.2060A>G	XP_011526271.1:p.Asp687Gly
XM_011527970.2:c.2093A>G	XP_011526272.1:p.Asp698Gly
XM_011527971.3:c.2093A>G	XP_011526273.1:p.Asp698Gly
XM_011527972.3:c.2093A>G	XP_011526274.1:p.Asp698Gly
XM_011527973.2:c.1973A>G	XP_011526275.1:p.Asp658Gly
XM_011527974.2:c.1961A>G	XP_011526276.1:p.Asp654Gly
XM_011527975.2:c.2060A>G	XP_011526277.1:p.Asp687Gly
XM_017026762.1:c.1358A>G	XP_016882251.1:p.Asp453Gly
NM_001290023.2:c.1940A>G	NP_001276952.1:p.Asp647Gly
NM_005535.3:c.1940A>G MANE Select	NP_005526.1:p.Asp647Gly