Canonical Allele Identifier: CA2676265606
Gene: IL12B HGNC NCBI

Linked Data

gnomAD v4: 5-159320646-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320646T>A , CM000667.2:g.159320646T>A GRCh38
NC_000005.9:g.158747654T>A , CM000667.1:g.158747654T>A GRCh37
NC_000005.8:g.158680232T>A NCBI36
NG_009618.1:g.14828A>T , LRG_71:g.14828A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-126A>T ENSP00000512849.1:n.-148-126A>T
ENST00000696751.1:c.365-126A>T ENSP00000512850.1:n.365-126A>T
ENST00000231228.3:c.483-126A>T MANE Select ENSP00000231228.2:n.483-126A>T
ENST00000231228.2:c.483-126A>T ENSP00000231228.2:n.483-126A>T
NM_002187.2:c.483-126A>T , LRG_71t1:c.483-126A>T NP_002178.2:n.483-126A>T
XR_001742945.1:n.147+50T>A
NM_002187.3:c.483-126A>T MANE Select NP_002178.2:n.483-126A>T
Search 100 bp 5'
Search 100 bp 3'