Canonical Allele Identifier: CA3538880

Gene: IL12B

Linked Data

• ExAC: 5:158750313 T / TAGGGTTAACACATAGGTCTTGTATTTATGGAAGTTGCTTTCTTACGGAAAGTCCAGGTGCATTGGACCAACAGCGA
• MyVariant Identifiers: chr5:g.158750313_158750314insAGGGTTAACACATAGGTCTTGTATTTATGGAAGTTGCTTTCTTACGGAAAGTCCAGGTGCATTGGACCAACAGCGA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159323306_159323307insGGGTTAACACATAGGTCTTGTATTTATGGAAGTTGCTTTCTTACGGAAAGTCCAGGTGCATTGGACCAACAGCGAA , CM000667.2:g.159323306_159323307insGGGTTAACACATAGGTCTTGTATTTATGGAAGTTGCTTTCTTACGGAAAGTCCAGGTGCATTGGACCAACAGCGAA	GRCh38
NC_000005.9:g.158750314_158750315insGGGTTAACACATAGGTCTTGTATTTATGGAAGTTGCTTTCTTACGGAAAGTCCAGGTGCATTGGACCAACAGCGAA , CM000667.1:g.158750314_158750315insGGGTTAACACATAGGTCTTGTATTTATGGAAGTTGCTTTCTTACGGAAAGTCCAGGTGCATTGGACCAACAGCGAA	GRCh37
NC_000005.8:g.158682892_158682893insGGGTTAACACATAGGTCTTGTATTTATGGAAGTTGCTTTCTTACGGAAAGTCCAGGTGCATTGGACCAACAGCGAA	NCBI36
NG_009618.1:g.12168_12169insTCGCTGTTGGTCCAATGCACCTGGACTTTCCGTAAGAAAGCAACTTCCATAAATACAAGACCTATGTGTTAACCCT , LRG_71:g.12168_12169insTCGCTGTTGGTCCAATGCACCTGGACTTTCCGTAAGAAAGCAACTTCCATAAATACAAGACCTATGTGTTAACCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-2786_-148-2785insTCGCTGTTGGTCCAATGCACCTGGACTTTCCGTAAGAAAGCAACTTCCATAAATACAAGACCTATGTGTTAACCCT	ENSP00000512849.1:n.-148-2786_-148-2785insTCGCTGTTGGTCCAATGCA...
ENST00000696751.1:c.112_113insTCGCTGTTGGTCCAATGCACCTGGACTTTCCGTAAGAAAGCAACTTCCATAAATACAAGACCTATGTGTTAACCCT	ENSP00000512850.1:p.Tyr38PhefsTer12
ENST00000231228.3:c.112_113insTCGCTGTTGGTCCAATGCACCTGGACTTTCCGTAAGAAAGCAACTTCCATAAATACAAGACCTATGTGTTAACCCT MANE Select	ENSP00000231228.2:p.Tyr38PhefsTer12
ENST00000231228.2:c.112_113insTCGCTGTTGGTCCAATGCACCTGGACTTTCCGTAAGAAAGCAACTTCCATAAATACAAGACCTATGTGTTAACCCT	ENSP00000231228.2:p.Tyr38PhefsTer12
NM_002187.2:c.112_113insTCGCTGTTGGTCCAATGCACCTGGACTTTCCGTAAGAAAGCAACTTCCATAAATACAAGACCTATGTGTTAACCCT , LRG_71t1:c.112_113insTCGCTGTTGGTCCAATGCACCTGGACTTTCCGTAAGAAAGCAACTTCCATAAATACAAGACCTATGTGTTAACCCT	NP_002178.2:p.Tyr38PhefsTer12
XR_001742945.1:n.148-2228_148-2227insGGGTTAACACATAGGTCTTGTATTTATGGAAGTTGCTTTCTTACGGAAAGTCCAGGTGCATTGGACCAACAGCGAA
NM_002187.3:c.112_113insTCGCTGTTGGTCCAATGCACCTGGACTTTCCGTAAGAAAGCAACTTCCATAAATACAAGACCTATGTGTTAACCCT MANE Select	NP_002178.2:p.Tyr38PhefsTer12