Canonical Allele Identifier: CA2676265373
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323440_159323442del , CM000667.2:g.159323440_159323442del GRCh38
NC_000005.9:g.158750448_158750450del , CM000667.1:g.158750448_158750450del GRCh37
NC_000005.8:g.158683026_158683028del NCBI36
NG_009618.1:g.12036_12038del , LRG_71:g.12036_12038del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2918_-148-2916del ENSP00000512849.1:n.-148-2918_-148-2916del
ENST00000696751.1:c.89-109_89-107del ENSP00000512850.1:n.89-109_89-107del
ENST00000231228.3:c.89-109_89-107del MANE Select ENSP00000231228.2:n.89-109_89-107del
ENST00000231228.2:c.89-109_89-107del ENSP00000231228.2:n.89-109_89-107del
NM_002187.2:c.89-109_89-107del , LRG_71t1:c.89-109_89-107del NP_002178.2:n.89-109_89-107del
XR_001742945.1:n.148-2094_148-2092del
NM_002187.3:c.89-109_89-107del MANE Select NP_002178.2:n.89-109_89-107del