Canonical Allele Identifier: CA362032734
Gene: IL12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.158747423G>T (hg19) chr5:g.159320415G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320415G>T , CM000667.2:g.159320415G>T GRCh38
NC_000005.9:g.158747423G>T , CM000667.1:g.158747423G>T GRCh37
NC_000005.8:g.158680001G>T NCBI36
NG_009618.1:g.15059C>A , LRG_71:g.15059C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-43C>A ENSP00000512849.1:n.-43C>A
ENST00000696751.1:c.*83C>A ENSP00000512850.1:n.*83C>A
ENST00000231228.3:c.588C>A MANE Select ENSP00000231228.2:p.Asp196Glu
ENST00000231228.2:c.588C>A ENSP00000231228.2:p.Asp196Glu
NM_002187.2:c.588C>A , LRG_71t1:c.588C>A NP_002178.2:p.Asp196Glu
NM_002187.3:c.588C>A MANE Select NP_002178.2:p.Asp196Glu
Search 100 bp 5'
Search 100 bp 3'