Canonical Allele Identifier: CA2676264646
Gene: IL12B HGNC NCBI

Linked Data

gnomAD v4: 5-159316199-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159316199G>T , CM000667.2:g.159316199G>T GRCh38
NC_000005.9:g.158743207G>T , CM000667.1:g.158743207G>T GRCh37
NC_000005.8:g.158675785G>T NCBI36
NG_009618.1:g.19275C>A , LRG_71:g.19275C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*1-99C>A ENSP00000512849.1:n.*1-99C>A
ENST00000696751.1:c.*483-99C>A ENSP00000512850.1:n.*483-99C>A
ENST00000231228.3:c.*1-99C>A MANE Select ENSP00000231228.2:n.*1-99C>A
ENST00000231228.2:c.*1-99C>A ENSP00000231228.2:n.*1-99C>A
NM_002187.2:c.*1-99C>A , LRG_71t1:c.*1-99C>A NP_002178.2:n.*1-99C>A
NM_002187.3:c.*1-99C>A MANE Select NP_002178.2:n.*1-99C>A
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