Canonical Allele Identifier: CA1083508472
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1470332261

Genomic Alleles

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

Transcript Alleles

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