Canonical Allele Identifier: CA362032484
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320357G>T , CM000667.2:g.159320357G>T GRCh38
NC_000005.9:g.158747365G>T , CM000667.1:g.158747365G>T GRCh37
NC_000005.8:g.158679943G>T NCBI36
NG_009618.1:g.15117C>A , LRG_71:g.15117C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.16C>A ENSP00000512849.1:p.His6Asn
ENST00000696751.1:c.*141C>A ENSP00000512850.1:n.*141C>A
ENST00000231228.3:c.646C>A MANE Select ENSP00000231228.2:p.His216Asn
ENST00000231228.2:c.646C>A ENSP00000231228.2:p.His216Asn
NM_002187.2:c.646C>A , LRG_71t1:c.646C>A NP_002178.2:p.His216Asn
NM_002187.3:c.646C>A MANE Select NP_002178.2:p.His216Asn