Canonical Allele Identifier: CA2573139335
Gene: IL12B HGNC NCBI

Linked Data

ClinVar Variation Id: 1366710
ClinVar RCV Id: RCV001930198
dbSNP Id: rs2113025865

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320301C>T , CM000667.2:g.159320301C>T GRCh38
NC_000005.9:g.158747309C>T , CM000667.1:g.158747309C>T GRCh37
NC_000005.8:g.158679887C>T NCBI36
NG_009618.1:g.15173G>A , LRG_71:g.15173G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.67+5G>A ENSP00000512849.1:n.67+5G>A
ENST00000696751.1:c.*192+5G>A ENSP00000512850.1:n.*192+5G>A
ENST00000231228.3:c.697+5G>A MANE Select ENSP00000231228.2:n.697+5G>A
ENST00000231228.2:c.697+5G>A ENSP00000231228.2:n.697+5G>A
NM_002187.2:c.697+5G>A , LRG_71t1:c.697+5G>A NP_002178.2:n.697+5G>A
NM_002187.3:c.697+5G>A MANE Select NP_002178.2:n.697+5G>A