Canonical Allele Identifier: CA1595018038
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159322026T= , CM000667.2:g.159322026T= GRCh38
NC_000005.9:g.158749034T= , CM000667.1:g.158749034T= GRCh37
NC_000005.8:g.158681612T= NCBI36
NG_009618.1:g.13448A= , LRG_71:g.13448A=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-1506A= ENSP00000512849.1:n.-148-1506A=
ENST00000696751.1:c.364+1028A= ENSP00000512850.1:n.364+1028A=
ENST00000231228.3:c.482+368A= MANE Select ENSP00000231228.2:n.482+368A=
ENST00000231228.2:c.482+368A= ENSP00000231228.2:n.482+368A=
NM_002187.2:c.482+368A= , LRG_71t1:c.482+368A= NP_002178.2:n.482+368A=
XR_001742945.1:n.147+1430T=
NM_002187.3:c.482+368A= MANE Select NP_002178.2:n.482+368A=