Canonical Allele Identifier: CA1595018455
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1562113441

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323034A>G , CM000667.2:g.159323034A>G GRCh38
NC_000005.9:g.158750042A>G , CM000667.1:g.158750042A>G GRCh37
NC_000005.8:g.158682620A>G NCBI36
NG_009618.1:g.12440T>C , LRG_71:g.12440T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-2514T>C ENSP00000512849.1:n.-148-2514T>C
ENST00000696751.1:c.364+20T>C ENSP00000512850.1:n.364+20T>C
ENST00000231228.3:c.364+20T>C MANE Select ENSP00000231228.2:n.364+20T>C
ENST00000231228.2:c.364+20T>C ENSP00000231228.2:n.364+20T>C
NM_002187.2:c.364+20T>C , LRG_71t1:c.364+20T>C NP_002178.2:n.364+20T>C
XR_001742945.1:n.147+2438A>G
NM_002187.3:c.364+20T>C MANE Select NP_002178.2:n.364+20T>C