Canonical Allele Identifier: CA1595018037
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159322022T= , CM000667.2:g.159322022T= GRCh38
NC_000005.9:g.158749030T= , CM000667.1:g.158749030T= GRCh37
NC_000005.8:g.158681608T= NCBI36
NG_009618.1:g.13452A= , LRG_71:g.13452A=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-1502A= ENSP00000512849.1:n.-148-1502A=
ENST00000696751.1:c.364+1032A= ENSP00000512850.1:n.364+1032A=
ENST00000231228.3:c.482+372A= MANE Select ENSP00000231228.2:n.482+372A=
ENST00000231228.2:c.482+372A= ENSP00000231228.2:n.482+372A=
NM_002187.2:c.482+372A= , LRG_71t1:c.482+372A= NP_002178.2:n.482+372A=
XR_001742945.1:n.147+1426T=
NM_002187.3:c.482+372A= MANE Select NP_002178.2:n.482+372A=