Canonical Allele Identifier: CA129826462
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1038879390
MyVariant Identifiers: chr5:g.158747021C>G (hg19) chr5:g.159320013C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320013C>G , CM000667.2:g.159320013C>G GRCh38
NC_000005.9:g.158747021C>G , CM000667.1:g.158747021C>G GRCh37
NC_000005.8:g.158679599C>G NCBI36
NG_009618.1:g.15461G>C , LRG_71:g.15461G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.67+293G>C ENSP00000512849.1:n.67+293G>C
ENST00000696751.1:c.*192+293G>C ENSP00000512850.1:n.*192+293G>C
ENST00000231228.3:c.697+293G>C MANE Select ENSP00000231228.2:n.697+293G>C
ENST00000231228.2:c.697+293G>C ENSP00000231228.2:n.697+293G>C
NM_002187.2:c.697+293G>C , LRG_71t1:c.697+293G>C NP_002178.2:n.697+293G>C
NM_002187.3:c.697+293G>C MANE Select NP_002178.2:n.697+293G>C
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