Canonical Allele Identifier: CA2676266171
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159322653_159322661dup , CM000667.2:g.159322653_159322661dup GRCh38
NC_000005.9:g.158749661_158749669dup , CM000667.1:g.158749661_158749669dup GRCh37
NC_000005.8:g.158682239_158682247dup NCBI36
NG_009618.1:g.12813_12821dup , LRG_71:g.12813_12821dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2141_-148-2133dup ENSP00000512849.1:n.-148-2141_-148-2133dup
ENST00000696751.1:c.364+393_364+401dup ENSP00000512850.1:n.364+393_364+401dup
ENST00000231228.3:c.365-150_365-142dup MANE Select ENSP00000231228.2:n.365-150_365-142dup
ENST00000231228.2:c.365-150_365-142dup ENSP00000231228.2:n.365-150_365-142dup
NM_002187.2:c.365-150_365-142dup , LRG_71t1:c.365-150_365-142dup NP_002178.2:n.365-150_365-142dup
XR_001742945.1:n.147+2057_147+2065dup
NM_002187.3:c.365-150_365-142dup MANE Select NP_002178.2:n.365-150_365-142dup