Canonical Allele Identifier: CA129826948
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs867995975

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320509G>A , CM000667.2:g.159320509G>A GRCh38
NC_000005.9:g.158747517G>A , CM000667.1:g.158747517G>A GRCh37
NC_000005.8:g.158680095G>A NCBI36
NG_009618.1:g.14965C>T , LRG_71:g.14965C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-137C>T ENSP00000512849.1:n.-137C>T
ENST00000696751.1:c.376C>T ENSP00000512850.1:p.Pro126Ser
ENST00000231228.3:c.494C>T MANE Select ENSP00000231228.2:p.Pro165Leu
ENST00000231228.2:c.494C>T ENSP00000231228.2:p.Pro165Leu
NM_002187.2:c.494C>T , LRG_71t1:c.494C>T NP_002178.2:p.Pro165Leu
XR_001742945.1:n.60G>A
NM_002187.3:c.494C>T MANE Select NP_002178.2:p.Pro165Leu