Canonical Allele Identifier: CA2676265752
Gene: IL12B HGNC NCBI

Linked Data

gnomAD v4: 5-159326794-GAGAGAAGCAGGGGGA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159326802_159326816del , CM000667.2:g.159326802_159326816del GRCh38
NC_000005.9:g.158753810_158753824del , CM000667.1:g.158753810_158753824del GRCh37
NC_000005.8:g.158686388_158686402del NCBI36
NG_009618.1:g.8665_8679del , LRG_71:g.8665_8679del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-149+3623_-149+3637del ENSP00000512849.1:n.-149+3623_-149+3637del
ENST00000696751.1:c.1-27_1-13del ENSP00000512850.1:n.1-27_1-13del
ENST00000696752.1:n.433-27_433-13del
ENST00000231228.3:c.1-27_1-13del MANE Select ENSP00000231228.2:n.1-27_1-13del
ENST00000231228.2:c.1-27_1-13del ENSP00000231228.2:n.1-27_1-13del
NM_002187.2:c.1-27_1-13del , LRG_71t1:c.1-27_1-13del NP_002178.2:n.1-27_1-13del
NM_002187.3:c.1-27_1-13del MANE Select NP_002178.2:n.1-27_1-13del
Search 100 bp 5'
Search 100 bp 3'