Canonical Allele Identifier: CA564025457
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1319195627
gnomAD v2: 5-158755424-C-CTGAGCCTCAGTCTCTTTGTCTATAAAA
gnomAD v3: 5-159328416-C-CTGAGCCTCAGTCTCTTTGTCTATAAAA
gnomAD v4: 5-159328416-C-CTGAGCCTCAGTCTCTTTGTCTATAAAA
MyVariant Identifiers: chr5:g.158755424_158755425insTGAGCCTCAGTCTCTTTGTCTATAAAA (hg19) chr5:g.159328416_159328417insTGAGCCTCAGTCTCTTTGTCTATAAAA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159328419_159328445dup , CM000667.2:g.159328419_159328445dup GRCh38
NC_000005.9:g.158755427_158755453dup , CM000667.1:g.158755427_158755453dup GRCh37
NC_000005.8:g.158688005_158688031dup NCBI36
NG_009618.1:g.7031_7057dup , LRG_71:g.7031_7057dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-149+1989_-149+2015dup ENSP00000512849.1:n.-149+1989_-149+2015dup
ENST00000696751.1:c.1-1661_1-1635dup ENSP00000512850.1:n.1-1661_1-1635dup
ENST00000696752.1:n.433-1661_433-1635dup
ENST00000231228.3:c.1-1661_1-1635dup MANE Select ENSP00000231228.2:n.1-1661_1-1635dup
ENST00000231228.2:c.1-1661_1-1635dup ENSP00000231228.2:n.1-1661_1-1635dup
NM_002187.2:c.1-1661_1-1635dup , LRG_71t1:c.1-1661_1-1635dup NP_002178.2:n.1-1661_1-1635dup
NM_002187.3:c.1-1661_1-1635dup MANE Select NP_002178.2:n.1-1661_1-1635dup
Search 100 bp 5'
Search 100 bp 3'