Canonical Allele Identifier: CA362032935
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320465C>A , CM000667.2:g.159320465C>A GRCh38
NC_000005.9:g.158747473C>A , CM000667.1:g.158747473C>A GRCh37
NC_000005.8:g.158680051C>A NCBI36
NG_009618.1:g.15009G>T , LRG_71:g.15009G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-93G>T ENSP00000512849.1:n.-93G>T
ENST00000696751.1:c.*33G>T ENSP00000512850.1:n.*33G>T
ENST00000231228.3:c.538G>T MANE Select ENSP00000231228.2:p.Val180Phe
ENST00000231228.2:c.538G>T ENSP00000231228.2:p.Val180Phe
NM_002187.2:c.538G>T , LRG_71t1:c.538G>T NP_002178.2:p.Val180Phe
XR_001742945.1:n.16C>A
NM_002187.3:c.538G>T MANE Select NP_002178.2:p.Val180Phe