Canonical Allele Identifier: CA2676265364
Gene: IL12B HGNC NCBI

Linked Data

gnomAD v4: 5-159323428-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323428C>T , CM000667.2:g.159323428C>T GRCh38
NC_000005.9:g.158750436C>T , CM000667.1:g.158750436C>T GRCh37
NC_000005.8:g.158683014C>T NCBI36
NG_009618.1:g.12046G>A , LRG_71:g.12046G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2908G>A ENSP00000512849.1:n.-148-2908G>A
ENST00000696751.1:c.89-99G>A ENSP00000512850.1:n.89-99G>A
ENST00000231228.3:c.89-99G>A MANE Select ENSP00000231228.2:n.89-99G>A
ENST00000231228.2:c.89-99G>A ENSP00000231228.2:n.89-99G>A
NM_002187.2:c.89-99G>A , LRG_71t1:c.89-99G>A NP_002178.2:n.89-99G>A
XR_001742945.1:n.148-2106C>T
NM_002187.3:c.89-99G>A MANE Select NP_002178.2:n.89-99G>A
Search 100 bp 5'
Search 100 bp 3'