Canonical Allele Identifier: CA2676265380
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323445_159323446del , CM000667.2:g.159323445_159323446del GRCh38
NC_000005.9:g.158750453_158750454del , CM000667.1:g.158750453_158750454del GRCh37
NC_000005.8:g.158683031_158683032del NCBI36
NG_009618.1:g.12029_12030del , LRG_71:g.12029_12030del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2925_-148-2924del ENSP00000512849.1:n.-148-2925_-148-2924del
ENST00000696751.1:c.89-116_89-115del ENSP00000512850.1:n.89-116_89-115del
ENST00000231228.3:c.89-116_89-115del MANE Select ENSP00000231228.2:n.89-116_89-115del
ENST00000231228.2:c.89-116_89-115del ENSP00000231228.2:n.89-116_89-115del
NM_002187.2:c.89-116_89-115del , LRG_71t1:c.89-116_89-115del NP_002178.2:n.89-116_89-115del
XR_001742945.1:n.148-2089_148-2088del
NM_002187.3:c.89-116_89-115del MANE Select NP_002178.2:n.89-116_89-115del