Canonical Allele Identifier: CA447510934
Gene: IL12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.158747387A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320379A>G , CM000667.2:g.159320379A>G GRCh38
NC_000005.9:g.158747387A>G , CM000667.1:g.158747387A>G GRCh37
NC_000005.8:g.158679965A>G NCBI36
NG_009618.1:g.15095T>C , LRG_71:g.15095T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-7T>C ENSP00000512849.1:n.-7T>C
ENST00000696751.1:c.*119T>C ENSP00000512850.1:n.*119T>C
ENST00000231228.3:c.624T>C MANE Select ENSP00000231228.2:p.Ile208=
ENST00000231228.2:c.624T>C ENSP00000231228.2:p.Ile208=
NM_002187.2:c.624T>C , LRG_71t1:c.624T>C NP_002178.2:p.Ile208=
NM_002187.3:c.624T>C MANE Select NP_002178.2:p.Ile208=
Search 100 bp 5'
Search 100 bp 3'