Canonical Allele Identifier: CA1595045713
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159316039T= , CM000667.2:g.159316039T= GRCh38
NC_000005.9:g.158743047T= , CM000667.1:g.158743047T= GRCh37
NC_000005.8:g.158675625T= NCBI36
NG_009618.1:g.19435A= , LRG_71:g.19435A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.*62A= ENSP00000512849.1:n.*62A=
ENST00000696751.1:c.*544A= ENSP00000512850.1:n.*544A=
ENST00000231228.3:c.*62A= MANE Select ENSP00000231228.2:n.*62A=
ENST00000231228.2:c.*62A= ENSP00000231228.2:n.*62A=
NM_002187.2:c.*62A= , LRG_71t1:c.*62A= NP_002178.2:n.*62A=
NM_002187.3:c.*62A= MANE Select NP_002178.2:n.*62A=