Canonical Allele Identifier: CA362032718
Gene: IL12B HGNC NCBI

Linked Data

gnomAD v4: 5-159320411-C-T
MyVariant Identifiers: chr5:g.158747419C>T (hg19) chr5:g.159320411C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320411C>T , CM000667.2:g.159320411C>T GRCh38
NC_000005.9:g.158747419C>T , CM000667.1:g.158747419C>T GRCh37
NC_000005.8:g.158679997C>T NCBI36
NG_009618.1:g.15063G>A , LRG_71:g.15063G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-39G>A ENSP00000512849.1:n.-39G>A
ENST00000696751.1:c.*87G>A ENSP00000512850.1:n.*87G>A
ENST00000231228.3:c.592G>A MANE Select ENSP00000231228.2:p.Ala198Thr
ENST00000231228.2:c.592G>A ENSP00000231228.2:p.Ala198Thr
NM_002187.2:c.592G>A , LRG_71t1:c.592G>A NP_002178.2:p.Ala198Thr
NM_002187.3:c.592G>A MANE Select NP_002178.2:p.Ala198Thr
Search 100 bp 5'
Search 100 bp 3'