Canonical Allele Identifier: CA129828606
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1010779225

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323122T>A , CM000667.2:g.159323122T>A GRCh38
NC_000005.9:g.158750130T>A , CM000667.1:g.158750130T>A GRCh37
NC_000005.8:g.158682708T>A NCBI36
NG_009618.1:g.12352A>T , LRG_71:g.12352A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-2602A>T ENSP00000512849.1:n.-148-2602A>T
ENST00000696751.1:c.296A>T ENSP00000512850.1:p.His99Leu
ENST00000231228.3:c.296A>T MANE Select ENSP00000231228.2:p.His99Leu
ENST00000231228.2:c.296A>T ENSP00000231228.2:p.His99Leu
NM_002187.2:c.296A>T , LRG_71t1:c.296A>T NP_002178.2:p.His99Leu
XR_001742945.1:n.148-2412T>A
NM_002187.3:c.296A>T MANE Select NP_002178.2:p.His99Leu