Canonical Allele Identifier: CA447511055
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1754067534
MyVariant Identifiers: chr5:g.158747465C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320457C>A , CM000667.2:g.159320457C>A GRCh38
NC_000005.9:g.158747465C>A , CM000667.1:g.158747465C>A GRCh37
NC_000005.8:g.158680043C>A NCBI36
NG_009618.1:g.15017G>T , LRG_71:g.15017G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-85G>T ENSP00000512849.1:n.-85G>T
ENST00000696751.1:c.*41G>T ENSP00000512850.1:n.*41G>T
ENST00000231228.3:c.546G>T MANE Select ENSP00000231228.2:p.Gly182=
ENST00000231228.2:c.546G>T ENSP00000231228.2:p.Gly182=
NM_002187.2:c.546G>T , LRG_71t1:c.546G>T NP_002178.2:p.Gly182=
XR_001742945.1:n.8C>A
NM_002187.3:c.546G>T MANE Select NP_002178.2:p.Gly182=