Canonical Allele Identifier: CA1083490736
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1754207944
gnomAD v3: 5-159327316-A-T
gnomAD v4: 5-159327316-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159327316A>T , CM000667.2:g.159327316A>T GRCh38
NC_000005.9:g.158754324A>T , CM000667.1:g.158754324A>T GRCh37
NC_000005.8:g.158686902A>T NCBI36
NG_009618.1:g.8158T>A , LRG_71:g.8158T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-149+3116T>A ENSP00000512849.1:n.-149+3116T>A
ENST00000696751.1:c.1-534T>A ENSP00000512850.1:n.1-534T>A
ENST00000696752.1:n.433-534T>A
ENST00000231228.3:c.1-534T>A MANE Select ENSP00000231228.2:n.1-534T>A
ENST00000231228.2:c.1-534T>A ENSP00000231228.2:n.1-534T>A
NM_002187.2:c.1-534T>A , LRG_71t1:c.1-534T>A NP_002178.2:n.1-534T>A
NM_002187.3:c.1-534T>A MANE Select NP_002178.2:n.1-534T>A
Search 100 bp 5'
Search 100 bp 3'