Canonical Allele Identifier: CA2676264595
Gene: IL12B HGNC NCBI

Linked Data

gnomAD v4: 5-159316077-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159316077C>T , CM000667.2:g.159316077C>T GRCh38
NC_000005.9:g.158743085C>T , CM000667.1:g.158743085C>T GRCh37
NC_000005.8:g.158675663C>T NCBI36
NG_009618.1:g.19397G>A , LRG_71:g.19397G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*24G>A ENSP00000512849.1:n.*24G>A
ENST00000696751.1:c.*506G>A ENSP00000512850.1:n.*506G>A
ENST00000231228.3:c.*24G>A MANE Select ENSP00000231228.2:n.*24G>A
ENST00000231228.2:c.*24G>A ENSP00000231228.2:n.*24G>A
NM_002187.2:c.*24G>A , LRG_71t1:c.*24G>A NP_002178.2:n.*24G>A
NM_002187.3:c.*24G>A MANE Select NP_002178.2:n.*24G>A
Search 100 bp 5'
Search 100 bp 3'