Canonical Allele Identifier: CA2676264559
Gene: IL12B HGNC NCBI

Linked Data

gnomAD v4: 5-159315950-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159315950C>G , CM000667.2:g.159315950C>G GRCh38
NC_000005.9:g.158742958C>G , CM000667.1:g.158742958C>G GRCh37
NC_000005.8:g.158675536C>G NCBI36
NG_009618.1:g.19524G>C , LRG_71:g.19524G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*151G>C ENSP00000512849.1:n.*151G>C
ENST00000696751.1:c.*633G>C ENSP00000512850.1:n.*633G>C
ENST00000231228.3:c.*151G>C MANE Select ENSP00000231228.2:n.*151G>C
ENST00000231228.2:c.*151G>C ENSP00000231228.2:n.*151G>C
NM_002187.2:c.*151G>C , LRG_71t1:c.*151G>C NP_002178.2:n.*151G>C
NM_002187.3:c.*151G>C MANE Select NP_002178.2:n.*151G>C
Search 100 bp 5'
Search 100 bp 3'