Canonical Allele Identifier: CA806391020
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1470332261

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159322143G>T , CM000667.2:g.159322143G>T GRCh38
NC_000005.9:g.158749151G>T , CM000667.1:g.158749151G>T GRCh37
NC_000005.8:g.158681729G>T NCBI36
NG_009618.1:g.13331C>A , LRG_71:g.13331C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-1623C>A ENSP00000512849.1:n.-148-1623C>A
ENST00000696751.1:c.364+911C>A ENSP00000512850.1:n.364+911C>A
ENST00000231228.3:c.482+251C>A MANE Select ENSP00000231228.2:n.482+251C>A
ENST00000231228.2:c.482+251C>A ENSP00000231228.2:n.482+251C>A
NM_002187.2:c.482+251C>A , LRG_71t1:c.482+251C>A NP_002178.2:n.482+251C>A
XR_001742945.1:n.147+1547G>T
NM_002187.3:c.482+251C>A MANE Select NP_002178.2:n.482+251C>A