Canonical Allele Identifier: CA362033015
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320504C>G , CM000667.2:g.159320504C>G GRCh38
NC_000005.9:g.158747512C>G , CM000667.1:g.158747512C>G GRCh37
NC_000005.8:g.158680090C>G NCBI36
NG_009618.1:g.14970G>C , LRG_71:g.14970G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-132G>C ENSP00000512849.1:n.-132G>C
ENST00000696751.1:c.381G>C ENSP00000512850.1:p.Lys127Asn
ENST00000231228.3:c.499G>C MANE Select ENSP00000231228.2:p.Gly167Arg
ENST00000231228.2:c.499G>C ENSP00000231228.2:p.Gly167Arg
NM_002187.2:c.499G>C , LRG_71t1:c.499G>C NP_002178.2:p.Gly167Arg
XR_001742945.1:n.55C>G
NM_002187.3:c.499G>C MANE Select NP_002178.2:p.Gly167Arg