Canonical Allele Identifier: CA447511008
Gene: IL12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.158747417G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320409G>C , CM000667.2:g.159320409G>C GRCh38
NC_000005.9:g.158747417G>C , CM000667.1:g.158747417G>C GRCh37
NC_000005.8:g.158679995G>C NCBI36
NG_009618.1:g.15065C>G , LRG_71:g.15065C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-37C>G ENSP00000512849.1:n.-37C>G
ENST00000696751.1:c.*89C>G ENSP00000512850.1:n.*89C>G
ENST00000231228.3:c.594C>G MANE Select ENSP00000231228.2:p.Ala198=
ENST00000231228.2:c.594C>G ENSP00000231228.2:p.Ala198=
NM_002187.2:c.594C>G , LRG_71t1:c.594C>G NP_002178.2:p.Ala198=
NM_002187.3:c.594C>G MANE Select NP_002178.2:p.Ala198=