Canonical Allele Identifier: CA1595018075
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159322121G= , CM000667.2:g.159322121G= GRCh38
NC_000005.9:g.158749129G= , CM000667.1:g.158749129G= GRCh37
NC_000005.8:g.158681707G= NCBI36
NG_009618.1:g.13353C= , LRG_71:g.13353C=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-1601C= ENSP00000512849.1:n.-148-1601C=
ENST00000696751.1:c.364+933C= ENSP00000512850.1:n.364+933C=
ENST00000231228.3:c.482+273C= MANE Select ENSP00000231228.2:n.482+273C=
ENST00000231228.2:c.482+273C= ENSP00000231228.2:n.482+273C=
NM_002187.2:c.482+273C= , LRG_71t1:c.482+273C= NP_002178.2:n.482+273C=
XR_001742945.1:n.147+1525G=
NM_002187.3:c.482+273C= MANE Select NP_002178.2:n.482+273C=