Canonical Allele Identifier: CA2676264597
Gene: IL12B HGNC NCBI

Linked Data

gnomAD v4: 5-159316086-A-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159316086A>T , CM000667.2:g.159316086A>T GRCh38
NC_000005.9:g.158743094A>T , CM000667.1:g.158743094A>T GRCh37
NC_000005.8:g.158675672A>T NCBI36
NG_009618.1:g.19388T>A , LRG_71:g.19388T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*15T>A ENSP00000512849.1:n.*15T>A
ENST00000696751.1:c.*497T>A ENSP00000512850.1:n.*497T>A
ENST00000231228.3:c.*15T>A MANE Select ENSP00000231228.2:n.*15T>A
ENST00000231228.2:c.*15T>A ENSP00000231228.2:n.*15T>A
NM_002187.2:c.*15T>A , LRG_71t1:c.*15T>A NP_002178.2:n.*15T>A
NM_002187.3:c.*15T>A MANE Select NP_002178.2:n.*15T>A
Search 100 bp 5'
Search 100 bp 3'