Canonical Allele Identifier: CA564024645
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1204497045

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323008T>C , CM000667.2:g.159323008T>C GRCh38
NC_000005.9:g.158750016T>C , CM000667.1:g.158750016T>C GRCh37
NC_000005.8:g.158682594T>C NCBI36
NG_009618.1:g.12466A>G , LRG_71:g.12466A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-2488A>G ENSP00000512849.1:n.-148-2488A>G
ENST00000696751.1:c.364+46A>G ENSP00000512850.1:n.364+46A>G
ENST00000231228.3:c.364+46A>G MANE Select ENSP00000231228.2:n.364+46A>G
ENST00000231228.2:c.364+46A>G ENSP00000231228.2:n.364+46A>G
NM_002187.2:c.364+46A>G , LRG_71t1:c.364+46A>G NP_002178.2:n.364+46A>G
XR_001742945.1:n.147+2412T>C
NM_002187.3:c.364+46A>G MANE Select NP_002178.2:n.364+46A>G