Canonical Allele Identifier: CA1083490773
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1754211611
gnomAD v3: 5-159327502-C-CT
gnomAD v4: 5-159327502-C-CT
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159327503dup , CM000667.2:g.159327503dup GRCh38
NC_000005.9:g.158754511dup , CM000667.1:g.158754511dup GRCh37
NC_000005.8:g.158687089dup NCBI36
NG_009618.1:g.7971dup , LRG_71:g.7971dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-149+2929dup ENSP00000512849.1:n.-149+2929dup
ENST00000696751.1:c.1-721dup ENSP00000512850.1:n.1-721dup
ENST00000696752.1:n.433-721dup
ENST00000231228.3:c.1-721dup MANE Select ENSP00000231228.2:n.1-721dup
ENST00000231228.2:c.1-721dup ENSP00000231228.2:n.1-721dup
NM_002187.2:c.1-721dup , LRG_71t1:c.1-721dup NP_002178.2:n.1-721dup
NM_002187.3:c.1-721dup MANE Select NP_002178.2:n.1-721dup
Search 100 bp 5'
Search 100 bp 3'