Canonical Allele Identifier: CA2676265698
Gene: IL12B HGNC NCBI

Linked Data

gnomAD v4: 5-159322293-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159322293T>C , CM000667.2:g.159322293T>C GRCh38
NC_000005.9:g.158749301T>C , CM000667.1:g.158749301T>C GRCh37
NC_000005.8:g.158681879T>C NCBI36
NG_009618.1:g.13181A>G , LRG_71:g.13181A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-1773A>G ENSP00000512849.1:n.-148-1773A>G
ENST00000696751.1:c.364+761A>G ENSP00000512850.1:n.364+761A>G
ENST00000231228.3:c.482+101A>G MANE Select ENSP00000231228.2:n.482+101A>G
ENST00000231228.2:c.482+101A>G ENSP00000231228.2:n.482+101A>G
NM_002187.2:c.482+101A>G , LRG_71t1:c.482+101A>G NP_002178.2:n.482+101A>G
XR_001742945.1:n.147+1697T>C
NM_002187.3:c.482+101A>G MANE Select NP_002178.2:n.482+101A>G
Search 100 bp 5'
Search 100 bp 3'