Canonical Allele Identifier: CA2676265471
Gene: IL12B HGNC NCBI

Linked Data

gnomAD v4: 5-159320545-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320545C>T , CM000667.2:g.159320545C>T GRCh38
NC_000005.9:g.158747553C>T , CM000667.1:g.158747553C>T GRCh37
NC_000005.8:g.158680131C>T NCBI36
NG_009618.1:g.14929G>A , LRG_71:g.14929G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-25G>A ENSP00000512849.1:n.-148-25G>A
ENST00000696751.1:c.365-25G>A ENSP00000512850.1:n.365-25G>A
ENST00000231228.3:c.483-25G>A MANE Select ENSP00000231228.2:n.483-25G>A
ENST00000231228.2:c.483-25G>A ENSP00000231228.2:n.483-25G>A
NM_002187.2:c.483-25G>A , LRG_71t1:c.483-25G>A NP_002178.2:n.483-25G>A
XR_001742945.1:n.96C>T
NM_002187.3:c.483-25G>A MANE Select NP_002178.2:n.483-25G>A
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