Canonical Allele Identifier: CA362032772
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320423G>A , CM000667.2:g.159320423G>A GRCh38
NC_000005.9:g.158747431G>A , CM000667.1:g.158747431G>A GRCh37
NC_000005.8:g.158680009G>A NCBI36
NG_009618.1:g.15051C>T , LRG_71:g.15051C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-51C>T ENSP00000512849.1:n.-51C>T
ENST00000696751.1:c.*75C>T ENSP00000512850.1:n.*75C>T
ENST00000231228.3:c.580C>T MANE Select ENSP00000231228.2:p.Gln194Ter
ENST00000231228.2:c.580C>T ENSP00000231228.2:p.Gln194Ter
NM_002187.2:c.580C>T , LRG_71t1:c.580C>T NP_002178.2:p.Gln194Ter
NM_002187.3:c.580C>T MANE Select NP_002178.2:p.Gln194Ter