Canonical Allele Identifier: CA2676265368
Gene: IL12B HGNC NCBI

Linked Data

gnomAD v4: 5-159323432-GT-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323435del , CM000667.2:g.159323435del GRCh38
NC_000005.9:g.158750443del , CM000667.1:g.158750443del GRCh37
NC_000005.8:g.158683021del NCBI36
NG_009618.1:g.12041del , LRG_71:g.12041del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2913del ENSP00000512849.1:n.-148-2913del
ENST00000696751.1:c.89-104del ENSP00000512850.1:n.89-104del
ENST00000231228.3:c.89-104del MANE Select ENSP00000231228.2:n.89-104del
ENST00000231228.2:c.89-104del ENSP00000231228.2:n.89-104del
NM_002187.2:c.89-104del , LRG_71t1:c.89-104del NP_002178.2:n.89-104del
XR_001742945.1:n.148-2099del
NM_002187.3:c.89-104del MANE Select NP_002178.2:n.89-104del
Search 100 bp 5'
Search 100 bp 3'