Canonical Allele Identifier: CA2676265595
Gene: IL12B HGNC NCBI

Linked Data

gnomAD v4: 5-159320638-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320638T>G , CM000667.2:g.159320638T>G GRCh38
NC_000005.9:g.158747646T>G , CM000667.1:g.158747646T>G GRCh37
NC_000005.8:g.158680224T>G NCBI36
NG_009618.1:g.14836A>C , LRG_71:g.14836A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-118A>C ENSP00000512849.1:n.-148-118A>C
ENST00000696751.1:c.365-118A>C ENSP00000512850.1:n.365-118A>C
ENST00000231228.3:c.483-118A>C MANE Select ENSP00000231228.2:n.483-118A>C
ENST00000231228.2:c.483-118A>C ENSP00000231228.2:n.483-118A>C
NM_002187.2:c.483-118A>C , LRG_71t1:c.483-118A>C NP_002178.2:n.483-118A>C
XR_001742945.1:n.147+42T>G
NM_002187.3:c.483-118A>C MANE Select NP_002178.2:n.483-118A>C
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