Canonical Allele Identifier: CA2570048947
Gene: IL12B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159322130A>G , CM000667.2:g.159322130A>G GRCh38
NC_000005.9:g.158749138A>G , CM000667.1:g.158749138A>G GRCh37
NC_000005.8:g.158681716A>G NCBI36
NG_009618.1:g.13344T>C , LRG_71:g.13344T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-1610T>C ENSP00000512849.1:n.-148-1610T>C
ENST00000696751.1:c.364+924T>C ENSP00000512850.1:n.364+924T>C
ENST00000231228.3:c.482+264T>C MANE Select ENSP00000231228.2:n.482+264T>C
ENST00000231228.2:c.482+264T>C ENSP00000231228.2:n.482+264T>C
NM_002187.2:c.482+264T>C , LRG_71t1:c.482+264T>C NP_002178.2:n.482+264T>C
XR_001742945.1:n.147+1534A>G
NM_002187.3:c.482+264T>C MANE Select NP_002178.2:n.482+264T>C
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