Canonical Allele Identifier: CA447511065
Gene: IL12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.158747471G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320463G>T , CM000667.2:g.159320463G>T GRCh38
NC_000005.9:g.158747471G>T , CM000667.1:g.158747471G>T GRCh37
NC_000005.8:g.158680049G>T NCBI36
NG_009618.1:g.15011C>A , LRG_71:g.15011C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-91C>A ENSP00000512849.1:n.-91C>A
ENST00000696751.1:c.*35C>A ENSP00000512850.1:n.*35C>A
ENST00000231228.3:c.540C>A MANE Select ENSP00000231228.2:p.Val180=
ENST00000231228.2:c.540C>A ENSP00000231228.2:p.Val180=
NM_002187.2:c.540C>A , LRG_71t1:c.540C>A NP_002178.2:p.Val180=
XR_001742945.1:n.14G>T
NM_002187.3:c.540C>A MANE Select NP_002178.2:p.Val180=